Atrophy of GingivaNCT06057363
Volumetric Evaluation of Gingival Augmentation Around Dental Implants
An observational study of Atrophy of Gingiva, run by Odontostomatologic Laser Therapy Center, Florence, Italy at 1 site in Italy.
Trial summary
The goal of this observational prospective study is to objectively assess the dimensional (volume \& linear variance) and clinical changes of vestibular gingival soft tissues upon treatment with laser-aided pouch roll augmentation technique and implant placement over a 12-month follow-up. Read more about this study
- Who is it for?
- Ages 42 to 86 yearsHealthy volunteers can take part
- Conditions the study is for
- Atrophy of Gingiva
- What is being tested?
- volumetric evaluation of gingival augmentation around dental implants
- How many people
- 12 participants
- Where
- 1 siteItaly
- Study dates
- 1 Mar 2022to 1 Sep 2023
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 42 to 86 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: 12 partially edentulous patients (mean age 62; range 42-86; 9 males/5 females) requiring vestibular soft tissue augmentation at implant sites in second-stage surgery because of mild horizontal ridge deficiency were enrolled
Who may be able to join
- Age > 18 years.
- Self-reported smoking habits >10 cigarettes/day.
- Full-mouth plaque score and full-mouth bleeding score ≤15%, measured at four sites per tooth.
- Need for aesthetic and/or functional soft tissue augmentation in single or multiple implant sites at the upper and/or lower quadrants.
Who cannot join
- Diseases affecting connective tissue metabolism.
- Uncontrolled diabetes (glycated hemoglobin HbA1c >7).
- Pregnant or lactating women.
- Untreated periodontal disease.
- Heavy gingival pigmentation (grade 3 Dummet Oral Pigmentation Index) requiring substantially different photoablative laser settings
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Volumetric and Clinical Evaluation of Peri-implant Soft Tissue Augmentation in Different Sites After Laser-aided Pouch Roll Technique: a Prospective Study
The goal of this observational prospective study is to objectively assess the dimensional (volume \& linear variance) and clinical changes of vestibular gingival soft tissues upon treatment with laser-aided pouch roll augmentation technique and implant placement over a 12-month follow-up. Twelve patients with 16 mild horizontal ridge deficiencies in different edentulous sites scheduled for implant placement were enrolled. Digital impressions were taken with an intra-oral laser scanner and software and analyzed before (day 0) and 12 months after laser-aided pouch roll augmentation surgery. The digital files were converted to STL format and superimposed to assess peri-implant volumetric and linear dimensional variations in selected regions of interest (ROI) by a 3D analysis software. Operator-assessed clinical periodontal parameters (probing depth PD, bleeding on probing BoP, plaque index PI) were recorded. Patient-reported outcome (pain, discomfort, treatment liking) and aesthetic result were evaluated by administration of appropriate questionnaires.
Read the detailed description
Introduction Adequate soft tissue thickness at the vestibular aspect of dental implants are crucial for satisfactory implant engraftment and aesthetic outcome. To pursue this objective, numerous surgical procedures have been adopted to augment the peri-implant gingiva, including autologous soft tissue grafting, xenogeneic collagen matrix, acellular dermal matrix, and roll/pedicle flap techniques: however, the available data do not suffice to clearly indicate which technique yields the best results.
The pouch roll techniques, originally proposed by Abrams in 1980 and subsequently improved, are particularly effective because they maintain vascularity of the grafted flap, which greatly facilitates its survival. Most of these procedures use a scalpel to shape the flap and remove the keratinized epithelial layer, but this conventional pouch roll technique is hampered by the fact that flap thickness must be no less than 3 mm and it is very difficult to perform hand scalpel gingival de-epithelization of the without damaging the underlying connective tissue, thereby causing bleeding and predisposing to scarring in the long term. More recently, laser-aided epithelial photoablation has been proposed as a possible solution to these issues. In fact, diode laser operating at 810 nm wavelength (λ) has been successfully used for selective de-epithelialization for several periodontal therapy purposes, e.g. palatal grafts for gingival recession defects, gingival hyperpigmentation, intra/extra pocket decontamination in chronic periodontitis and placement to second-stage surgery for buried implant exposure. Laser photoablation offers several advantages, namely excellent hemostasis that results in a dry surgical field and better view of the operative field, tissue surface sterilization and shallow penetration limited to the gingival epithelium with minimal injury and inflammation of the underlying lamina propria. On this ground, the investigators successfully combined diode laser photoablation (λ 810 nm) to conventional roll flap technique for mild vestibular ridge deficiencies: in a preliminary, limited series of patients (n=3) this improved method resulted in fast healing, satisfactory clinical and aesthetic results, rapid prosthetic restoration and no need for local or systemic analgesics. The present study aims on one hand at expanding the case series to consolidate the preliminary findings, on the other hand at evaluating another key clinical outcome parameter of this laser-aided roll flap procedure, namely the actual, objective gingival soft tissue augmentation over time. To this purpose, the volume of the treated regions, acquired by a digital intra-oral scanning, was measured and analyzed by appropriate 3D software and compared before roll flap surgery and implant placement and upon 12-month follow-up. Post-operative discomfort and aesthetic satisfaction of the patients were also assessed.
Material and methods
Volumetric measurements and analysis - Volume changes of the vestibular gingiva before and after the laser-aided roll-flap augmentation were evaluated and compared on digital intra-oral scanning impressions taken with an intra-oral scanner (Dentsply Syrona, Rome, Italy) and 3D reconstruction software (Exocad, Darmstadt, Germany). To reduce possible deviations and ensure higher accuracy of 3D analysis, quadrant instead of full-arch scans were recorded. These were converted to standard tessellation language (STL) format. Pre and post-operative STL files were collected, aligned and superimposed by selecting 10 reproducible anatomical points as landmarks prior to be analyzed with an appropriate software (Rhyno3D, Washington DC, USA). This software allowed: i) to demarcate an exact 3D region of interest (ROI), ii) to superimpose the same ROI taken at 2 time points, i.e. before surgery (day 0) and at 12-month follow-up, while to measure the volume of the 2 corresponding ROI and to objectively assess their differences at the different time points. Each selected ROI corresponded to a single or multiple implant site. According to previous studies, ROI in the single implant sites was demarcated on the vestibular gingival aspect using the following criteria:
- gingiva-to-implant margin (or coronal gingival ridge, if before implant placement) as horizontal coronal border;
- muco-gingival junction as horizontal apical border;
- two vertical lines, 2 mm aside the surgical flap incision and corresponding to the mid-point of the interdental papillas, as mesial and distal borders.
Due to individual variations in oral anatomy, ROI were obviously different among the patients, but substantially identical in the same patient at successive time points. The software was set to a spatial resolution of ±50 nm between the STL files: in this way, negligible or no variations <50 nm in the merged STL file appeared green in a visual pseudo-color range. To assess reproducibility of the method, a trained blinded examiner (M.P.), performed 2 measurements at 1-week interval: intra-class correlation coefficient was 0.87 (95% CI 0.82-0.91).
In each patient, the 2 ROI volumes (cubic mm) measured at day 0 and 12 months were compared to evaluate the changes of the vestibular gingival soft tissue over time. Exocad software also allowed to determine the linear dimensional changes (LD), i.e. the linear distance (mm) between the 2 ROI surfaces measured at 1, 3 and 5 mm along a vertical midline traced between the gingival free margin and the muco-gingival junction, as previously reported.
Clinical peri-implant parameters and calibration - At 12 months, a trained and blinded examiner (L.L.) evaluated PD and BoP (within 30 s after probing) at 6 sites per implant (3 buccal, 3 palatal) and PI (yes/no, 4 sites per implant), using a conventional manual periodontal probe (PCP15, Hu-Friedy, Milan, Italy) with about a 0.3 N force. Operator calibration was considered satisfactory when the percent fitting between the first and second measurements taken at a 24-h gap was ≥ 90%.
Primary outcome variables
- Objectively measurable volumetric changes (cubic mm) of the ROI regions between day 0 and 12 months.
- Objectively measurable linear dimensional changes (LD, mm) of the ROI regions between day 0 and 12 months;
Secondary outcome variables
- Changes in periodontal probing depth PD (mm)
- Changes in periodontal bleeding on probing BoP (yes/no),
- Changes in plaque index PI (yes/no)
- Subjective perception of discomfort and pain during surgery and the post-operative period, semi-quantitatively assessed by Visual Analogue Scale (VAS) questionnaires administered 5 h after surgery and each morning for the next 7 days (score: 0,no pain to 10,extremely painful);
- analgesics taken (number);
- willingness to undergo the same treatment again (yes/no).
- Color and texture differences between peri-implant and natural gingiva at 12 months, subjectively evaluated by the patients at a mirror from speaking distance (visible/not visible).
Operators - Laser-aided roll-flap technique was performed by a dental practitioner (M.G) with long-lasting expertise in periodontal surgery, implant dentistry and use of dental laser technology.
Surgical treatments - The delivered laser-aided roll flap technique was performed as previously described. It consisted in the following steps:
- De-epithelialization of a vestibular gingival area, 2 mm larger than the cover screw diameter, using a λ 810-nm diode GaAlAs laser (4x4 Dental Laser System, General Project Ltd., Montespertoli, Florence, Italy) equipped with a ∅ 600-μm optical fiber and set as follows: pulse mode, frequency 8,000 Hz, pulse energy 69 μJ, pulse duration 18 μs, corresponding to 0.6 W
- mean power (peak 3.8 W) and 40 J/square cm irradiation energy. Photoablation was performed in fiber tip contact mode at a constant speed of about 2.5 mm/s under airflow cooling and thermographic feedback to prevent tissue over-heating and damage. The procedure was made under a high-resolution stereomicroscope (Extaro 300, Zeiss, Milan, Italy).
- Full-thickness U-shaped incision of the photoablated mucosa was made with the same λ 810-nm diode laser set at pulse energy 22 μJ, peak power 3.14 W, frequency 20 kHz, pulse width 7 μs, in contact mode and equipped with a ∅ 300-μm optical fiber. The incision margins were extended to the vestibular gingiva for 2 to 3 mm to facilitate flap displacement.
- Elevation and rolling of the full-thickness flap into a vestibular pouch, no surgical sutures.
- Relieve or remove any soft tissue or bone interferences by adjusting the abutment or the tissues.
- Connection of titanium abutments or healing abutment to the implants. Overall time of the surgical procedure was measured, starting from the end of local anesthesia to connection of titanium abutment.
Post-surgical instructions and prosthetic treatments - No local or systemic antibiotics, mouthwashes or toothpastes containing triclosan, chlorhexidine, or other disinfectants were prescribed. The patients were instructed to avoid brushing of the treated zone for about 6 hours from surgery and then to perform normal oral hygiene.
Prosthetic treatment including the application of a temporary crown and the final rehabilitation was performed according to a standard treatment plan.
Statistical analysis - This was performed with Prism5 software (GraphPad, Boston, MA, USA). The ROI of each treated implant/tooth site was taken as unit of analysis. Differences in ROI volumes (mean ±SEM) measured before the treatment (day 0) and at 12-month follow-up were analysed statistically by Student's t test for paired values. A p value ≤0.05 was considered significant.
- Conditions
- Atrophy of Gingiva
- Being tested
- volumetric evaluation of gingival augmentation around dental implants
- Keywords
- dental implants, roll flap, gingival augmentation, volume changes, linear dimensional changes, clinical periodontal parameters, patient-reported outcomes
- Medical subject headings
- Gingival Recession
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
volumetric evaluation of gingival augmentation around dental implantsOther
objective volumetric and clinical assesment of vestibular gingival soft tissues changes upon treatment with laser-aided pouch roll augmentation technique and implant placement over a 12-month follow-up
| Study group | Role | What they receive |
|---|---|---|
| patients requiring vestibular soft tissue augmentation at implant sites | The present study was planned as prospective analysis with 12-month follow-up. It enrolled 12 partially edentulous patients (mean age 62; range 42-86) requiring vestibular soft tissue augmentation at implant sites in second-stage surgery because of mild horizontal ridge deficiency. As a whole, 16 implants were placed (8 single, 4 dual). Receives: Other: volumetric evaluation of gingival augmentation around dental implants |
What is being measured
The primary outcome is the main question the study is designed to answer.
Objectively measurable volume changes of the vestibular gingiva
Assessment of peri-implant volumetric variations (cubic mm) in selected regions of interest (ROI) of the vestibular gingiva by a 3D analysis software
Measured: 12 months
Objectively measurable linear dimensional (LD) changes of the vestibular gingiva
Assessment of peri-implant linear dimensional variations (mm) at 3 vertical points (1,3,5 mm form the free margin) in selected regions of interest (ROI) of the vestibular gingiva by a 3D analysis software
Measured: 12 months
Secondary outcomes (7)
Changes in periodontal probing depth PD (mm)
Operator-assessed periodontal probing depth (PD), in mm
Measured: 12 months
Changes in periodontal bleeding on probing BoP
Operator-assessed periodontal bleeding on probing (BoP) within 30 s, 6 sites per implant (yes/no)
Measured: 12 months
Changes in periodontal plaque index PI
Operator-assessed periodontal plaque index, 4 sites per implant (yes/no)
Measured: 12 months
Subjective perception of discomfort and pain during surgery and the post-operative period
Patient-reported perception of discomfort and pain during surgery and the post-operative period, semi-quantitatively assessed by Visual Analogue Scale (VAS) questionnaires administered 5 h after surgery and each morning for the next 7 days (score: 0,no pain to 10,extremely painful)
Measured: 7 days
Analgesics taken
Patient-reported No. of pills of analgesics taken after surgery and in the next days
Measured: 7 days
Treatment liking
Patient-reported willingness to undergo the same treatment again (yes/no)
Measured: 7 days
Gingival color and texture appearance
Patient-reported color and texture differences between peri-implant and natural gingiva, subjectively evaluated at a mirror from speaking distance (visible/not visible).
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Sep 2023
- Study start1 Mar 2022
- Primary completion1 Mar 2023
- Study completion1 Sep 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (15)Papers the sponsor has linked to this study.
- Other trials for Atrophy of GingivaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 12 participants (actual)
Sponsor and investigators
- Lead sponsor
- Odontostomatologic Laser Therapy Center, Florence, Italy
- Sponsor type
- University, hospital or other
- Collaborators
- University of Florence
- Responsible party
- Sponsor
- Investigators
- Marco Giannelli, MD, Principal investigator, Odontostomatologic Laser Therapy Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06057363
- Sponsor's protocol ID
- 20546-oss
- Status last verified
- Sep 2023
- First submitted
- 13 Sep 2023
- Last updated
- 29 Sep 2023
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Abrams L. Augmentation of the deformed residual edentulous ridge for fixed prosthesis. Compend Contin Educ Gen Dent. 1980 May-Jun;1(3):205-13. No abstract available.
PubMed 6950834Bassetti RG, Stahli A, Bassetti MA, Sculean A. Soft tissue augmentation around osseointegrated and uncovered dental implants: a systematic review. Clin Oral Investig. 2017 Jan;21(1):53-70. doi: 10.1007/s00784-016-2007-9. Epub 2016 Nov 21.
PubMed 27873018El-Kholey KE. Efficacy and safety of a diode laser in second-stage implant surgery: a comparative study. Int J Oral Maxillofac Surg. 2014 May;43(5):633-8. doi: 10.1016/j.ijom.2013.10.003. Epub 2013 Nov 7.
PubMed 24210453Fons-Badal C, Alonso Perez-Barquero J, Martinez-Martinez N, Faus-Lopez J, Fons-Font A, Agustin-Panadero R. A novel, fully digital approach to quantifying volume gain after soft tissue graft surgery. A pilot study. J Clin Periodontol. 2020 May;47(5):614-620. doi: 10.1111/jcpe.13235. Epub 2020 Mar 12.
PubMed 31860133Fornaini C, Merigo E, Vescovi P, Bonanini M, Antonietti W, Leoci L, Lagori G, Meleti M. Different laser wavelengths comparison in the second-stage implant surgery: an ex vivo study. Lasers Med Sci. 2015 Aug;30(6):1631-9. doi: 10.1007/s10103-014-1623-3. Epub 2014 Jul 3.
PubMed 24989333Giannelli M, Formigli L, Bani D. Comparative evaluation of photoablative efficacy of erbium: yttrium-aluminium-garnet and diode laser for the treatment of gingival hyperpigmentation. A randomized split-mouth clinical trial. J Periodontol. 2014 Apr;85(4):554-61. doi: 10.1902/jop.2013.130219. Epub 2013 Jul 4.
PubMed 23826649Giannelli M, Formigli L, Lorenzini L, Bani D. Combined photoablative and photodynamic diode laser therapy as an adjunct to non-surgical periodontal treatment: a randomized split-mouth clinical trial. J Clin Periodontol. 2012 Oct;39(10):962-70. doi: 10.1111/j.1600-051X.2012.01925.x. Epub 2012 Jul 27.
PubMed 22834932Gonzalez-Martin O, Veltri M, Moraguez O, Belser UC. Quantitative three-dimensional methodology to assess volumetric and profilometric outcome of subepithelial connective tissue grafting at pontic sites: a prospective pilot study. Int J Periodontics Restorative Dent. 2014 Sep-Oct;34(5):673-9. doi: 10.11607/prd.1808.
PubMed 25171038Ozcelik O, Seydaoglu G, Haytac CM. Diode laser for harvesting de-epithelialized palatal graft in the treatment of gingival recession defects: a randomized clinical trial. J Clin Periodontol. 2016 Jan;43(1):63-71. doi: 10.1111/jcpe.12487. Epub 2016 Jan 21.
PubMed 26660000Park SH, Wang HL. Pouch roll technique for implant soft tissue augmentation: a variation of the modified roll technique. Int J Periodontics Restorative Dent. 2012 Jun;32(3):e116-21.
PubMed 22408781Parvini P, Galarraga-Vinueza ME, Obreja K, Magini RS, Sader R, Schwarz F. Prospective study assessing three-dimensional changes of mucosal healing following soft tissue augmentation using free gingival grafts. J Periodontol. 2021 Mar;92(3):400-408. doi: 10.1002/JPER.19-0640. Epub 2020 Aug 21.
PubMed 33448379Schmidt A, Klussmann L, Wostmann B, Schlenz MA. Accuracy of Digital and Conventional Full-Arch Impressions in Patients: An Update. J Clin Med. 2020 Mar 4;9(3):688. doi: 10.3390/jcm9030688.
PubMed 32143433Tavelli L, Barootchi S, Majzoub J, Siqueira R, Mendonca G, Wang HL. Volumetric changes at implant sites: A systematic appraisal of traditional methods and optical scanning-based digital technologies. J Clin Periodontol. 2021 Feb;48(2):315-334. doi: 10.1111/jcpe.13401. Epub 2020 Nov 18.
PubMed 33151586Thoma DS, Naenni N, Figuero E, Hammerle CHF, Schwarz F, Jung RE, Sanz-Sanchez I. Effects of soft tissue augmentation procedures on peri-implant health or disease: A systematic review and meta-analysis. Clin Oral Implants Res. 2018 Mar;29 Suppl 15:32-49. doi: 10.1111/clr.13114.
PubMed 29498129von Elm E, Altman DG, Egger M, Pocock SJ, Gotzsche PC, Vandenbroucke JP; STROBE Initiative. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: guidelines for reporting observational studies. Int J Surg. 2014 Dec;12(12):1495-9. doi: 10.1016/j.ijsu.2014.07.013. Epub 2014 Jul 18.
PubMed 25046131
Study at a glance
From the registry record, last updated by the sponsor on 29 Sep 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Volumetric and Clinical Evaluation of Peri-implant Soft Tissue Augmentation in Different Sites After Laser-aided Pouch Roll Technique: a Prospective Study
- ClinicalTrials.gov ID
- NCT06057363
- Acronym / sponsor ID
- 20546-oss
- Conditions
- Atrophy of Gingiva
- Keywords
- dental implants, roll flap, gingival augmentation, volume changes, linear dimensional changes, clinical periodontal parameters, patient-reported outcomes
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 12 participants (actual)
- Lead sponsor
- Odontostomatologic Laser Therapy Center, Florence, ItalyUniversity, hospital or other
- Collaborators
- University of Florence
- Study start
- 1 Mar 2022 (actual)
- Primary completion
- 1 Mar 2023 (actual)
- Study completion
- 1 Sep 2023 (actual)
- First posted
- 28 Sep 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this observational prospective study is to objectively assess the dimensional (volume \& linear variance) and clinical changes of vestibular gingival soft tissues upon treatment with laser-aided pouch roll augmentation technique and implant placement over a 12-month follow-up. Twelve patients with 16 mild horizontal ridge deficiencies in different edentulous sites scheduled for implant placement were enrolled. Digital impressions were taken with an intra-oral laser scanner and software and analyzed before (day 0) and 12 months after laser-aided pouch roll augmentation surgery. The digital files were converted to STL format and superimposed to assess peri-implant volumetric and linear dimensional variations in selected regions of interest (ROI) by a 3D analysis software. Operator-assessed clinical periodontal parameters (probing depth PD, bleeding on probing BoP, plaque index PI) were recorded. Patient-reported outcome (pain, discomfort, treatment liking) and aesthetic result were evaluated by administration of appropriate questionnaires.
Detailed description
Introduction Adequate soft tissue thickness at the vestibular aspect of dental implants are crucial for satisfactory implant engraftment and aesthetic outcome. To pursue this objective, numerous surgical procedures have been adopted to augment the peri-implant gingiva, including autologous soft tissue grafting, xenogeneic collagen matrix, acellular dermal matrix, and roll/pedicle flap techniques: however, the available data do not suffice to clearly indicate which technique yields the best results.
The pouch roll techniques, originally proposed by Abrams in 1980 and subsequently improved, are particularly effective because they maintain vascularity of the grafted flap, which greatly facilitates its survival. Most of these procedures use a scalpel to shape the flap and remove the keratinized epithelial layer, but this conventional pouch roll technique is hampered by the fact that flap thickness must be no less than 3 mm and it is very difficult to perform hand scalpel gingival de-epithelization of the without damaging the underlying connective tissue, thereby causing bleeding and predisposing to scarring in the long term. More recently, laser-aided epithelial photoablation has been proposed as a possible solution to these issues. In fact, diode laser operating at 810 nm wavelength (λ) has been successfully used for selective de-epithelialization for several periodontal therapy purposes, e.g. palatal grafts for gingival recession defects, gingival hyperpigmentation, intra/extra pocket decontamination in chronic periodontitis and placement to second-stage surgery for buried implant exposure. Laser photoablation offers several advantages, namely excellent hemostasis that results in a dry surgical field and better view of the operative field, tissue surface sterilization and shallow penetration limited to the gingival epithelium with minimal injury and inflammation of the underlying lamina propria. On this ground, the investigators successfully combined diode laser photoablation (λ 810 nm) to conventional roll flap technique for mild vestibular ridge deficiencies: in a preliminary, limited series of patients (n=3) this improved method resulted in fast healing, satisfactory clinical and aesthetic results, rapid prosthetic restoration and no need for local or systemic analgesics. The present study aims on one hand at expanding the case series to consolidate the preliminary findings, on the other hand at evaluating another key clinical outcome parameter of this laser-aided roll flap procedure, namely the actual, objective gingival soft tissue augmentation over time. To this purpose, the volume of the treated regions, acquired by a digital intra-oral scanning, was measured and analyzed by appropriate 3D software and compared before roll flap surgery and implant placement and upon 12-month follow-up. Post-operative discomfort and aesthetic satisfaction of the patients were also assessed.
Material and methods
Volumetric measurements and analysis - Volume changes of the vestibular gingiva before and after the laser-aided roll-flap augmentation were evaluated and compared on digital intra-oral scanning impressions taken with an intra-oral scanner (Dentsply Syrona, Rome, Italy) and 3D reconstruction software (Exocad, Darmstadt, Germany). To reduce possible deviations and ensure higher accuracy of 3D analysis, quadrant instead of full-arch scans were recorded. These were converted to standard tessellation language (STL) format. Pre and post-operative STL files were collected, aligned and superimposed by selecting 10 reproducible anatomical points as landmarks prior to be analyzed with an appropriate software (Rhyno3D, Washington DC, USA). This software allowed: i) to demarcate an exact 3D region of interest (ROI), ii) to superimpose the same ROI taken at 2 time points, i.e. before surgery (day 0) and at 12-month follow-up, while to measure the volume of the 2 corresponding ROI and to objectively assess their differences at the different time points. Each selected ROI corresponded to a single or multiple implant site. According to previous studies, ROI in the single implant sites was demarcated on the vestibular gingival aspect using the following criteria:
- gingiva-to-implant margin (or coronal gingival ridge, if before implant placement) as horizontal coronal border;
- muco-gingival junction as horizontal apical border;
- two vertical lines, 2 mm aside the surgical flap incision and corresponding to the mid-point of the interdental papillas, as mesial and distal borders.
Due to individual variations in oral anatomy, ROI were obviously different among the patients, but substantially identical in the same patient at successive time points. The software was set to a spatial resolution of ±50 nm between the STL files: in this way, negligible or no variations <50 nm in the merged STL file appeared green in a visual pseudo-color range. To assess reproducibility of the method, a trained blinded examiner (M.P.), performed 2 measurements at 1-week interval: intra-class correlation coefficient was 0.87 (95% CI 0.82-0.91).
In each patient, the 2 ROI volumes (cubic mm) measured at day 0 and 12 months were compared to evaluate the changes of the vestibular gingival soft tissue over time. Exocad software also allowed to determine the linear dimensional changes (LD), i.e. the linear distance (mm) between the 2 ROI surfaces measured at 1, 3 and 5 mm along a vertical midline traced between the gingival free margin and the muco-gingival junction, as previously reported.
Clinical peri-implant parameters and calibration - At 12 months, a trained and blinded examiner (L.L.) evaluated PD and BoP (within 30 s after probing) at 6 sites per implant (3 buccal, 3 palatal) and PI (yes/no, 4 sites per implant), using a conventional manual periodontal probe (PCP15, Hu-Friedy, Milan, Italy) with about a 0.3 N force. Operator calibration was considered satisfactory when the percent fitting between the first and second measurements taken at a 24-h gap was ≥ 90%.
Primary outcome variables
- Objectively measurable volumetric changes (cubic mm) of the ROI regions between day 0 and 12 months.
- Objectively measurable linear dimensional changes (LD, mm) of the ROI regions between day 0 and 12 months;
Secondary outcome variables
- Changes in periodontal probing depth PD (mm)
- Changes in periodontal bleeding on probing BoP (yes/no),
- Changes in plaque index PI (yes/no)
- Subjective perception of discomfort and pain during surgery and the post-operative period, semi-quantitatively assessed by Visual Analogue Scale (VAS) questionnaires administered 5 h after surgery and each morning for the next 7 days (score: 0,no pain to 10,extremely painful);
- analgesics taken (number);
- willingness to undergo the same treatment again (yes/no).
- Color and texture differences between peri-implant and natural gingiva at 12 months, subjectively evaluated by the patients at a mirror from speaking distance (visible/not visible).
Operators - Laser-aided roll-flap technique was performed by a dental practitioner (M.G) with long-lasting expertise in periodontal surgery, implant dentistry and use of dental laser technology.
Surgical treatments - The delivered laser-aided roll flap technique was performed as previously described. It consisted in the following steps:
- De-epithelialization of a vestibular gingival area, 2 mm larger than the cover screw diameter, using a λ 810-nm diode GaAlAs laser (4x4 Dental Laser System, General Project Ltd., Montespertoli, Florence, Italy) equipped with a ∅ 600-μm optical fiber and set as follows: pulse mode, frequency 8,000 Hz, pulse energy 69 μJ, pulse duration 18 μs, corresponding to 0.6 W
- mean power (peak 3.8 W) and 40 J/square cm irradiation energy. Photoablation was performed in fiber tip contact mode at a constant speed of about 2.5 mm/s under airflow cooling and thermographic feedback to prevent tissue over-heating and damage. The procedure was made under a high-resolution stereomicroscope (Extaro 300, Zeiss, Milan, Italy).
- Full-thickness U-shaped incision of the photoablated mucosa was made with the same λ 810-nm diode laser set at pulse energy 22 μJ, peak power 3.14 W, frequency 20 kHz, pulse width 7 μs, in contact mode and equipped with a ∅ 300-μm optical fiber. The incision margins were extended to the vestibular gingiva for 2 to 3 mm to facilitate flap displacement.
- Elevation and rolling of the full-thickness flap into a vestibular pouch, no surgical sutures.
- Relieve or remove any soft tissue or bone interferences by adjusting the abutment or the tissues.
- Connection of titanium abutments or healing abutment to the implants. Overall time of the surgical procedure was measured, starting from the end of local anesthesia to connection of titanium abutment.
Post-surgical instructions and prosthetic treatments - No local or systemic antibiotics, mouthwashes or toothpastes containing triclosan, chlorhexidine, or other disinfectants were prescribed. The patients were instructed to avoid brushing of the treated zone for about 6 hours from surgery and then to perform normal oral hygiene.
Prosthetic treatment including the application of a temporary crown and the final rehabilitation was performed according to a standard treatment plan.
Statistical analysis - This was performed with Prism5 software (GraphPad, Boston, MA, USA). The ROI of each treated implant/tooth site was taken as unit of analysis. Differences in ROI volumes (mean ±SEM) measured before the treatment (day 0) and at 12-month follow-up were analysed statistically by Student's t test for paired values. A p value ≤0.05 was considered significant.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| patients requiring vestibular soft tissue augmentation at implant sites | – | Other: volumetric evaluation of gingival augmentation around dental implantsThe present study was planned as prospective analysis with 12-month follow-up. It enrolled 12 partially edentulous patients (mean age 62; range 42-86) requiring vestibular soft tissue augmentation at implant sites in second-stage surgery because of mild horizontal ridge deficiency. As a whole, 16 implants were placed (8 single, 4 dual). |
Who may qualify
- Ages
- 42 to 86 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- 12 partially edentulous patients (mean age 62; range 42-86; 9 males/5 females) requiring vestibular soft tissue augmentation at implant sites in second-stage surgery because of mild horizontal ridge deficiency were enrolled
Key inclusion criteria (4 listed)
- Age > 18 years.
- Self-reported smoking habits >10 cigarettes/day.
- Full-mouth plaque score and full-mouth bleeding score ≤15%, measured at four sites per tooth.
- Need for aesthetic and/or functional soft tissue augmentation in single or multiple implant sites at the upper and/or lower quadrants.
Key exclusion criteria (5 listed)
- Diseases affecting connective tissue metabolism.
- Uncontrolled diabetes (glycated hemoglobin HbA1c >7).
- Pregnant or lactating women.
- Untreated periodontal disease.
- Heavy gingival pigmentation (grade 3 Dummet Oral Pigmentation Index) requiring substantially different photoablative laser settings
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| volumetric evaluation of gingival augmentation around dental implantsobjective volumetric and clinical assesment of vestibular gingival soft tissues changes upon treatment with laser-aided pouch roll augmentation technique and implant placement over a 12-month follow-up | Other | patients requiring vestibular soft tissue augmentation at implant sites |
Primary outcome
Objectively measurable volume changes of the vestibular gingiva
Time frame: 12 months
Assessment of peri-implant volumetric variations (cubic mm) in selected regions of interest (ROI) of the vestibular gingiva by a 3D analysis software
Objectively measurable linear dimensional (LD) changes of the vestibular gingiva
Time frame: 12 months
Assessment of peri-implant linear dimensional variations (mm) at 3 vertical points (1,3,5 mm form the free margin) in selected regions of interest (ROI) of the vestibular gingiva by a 3D analysis software
7 secondary outcomes
Changes in periodontal probing depth PD (mm)
Time frame: 12 months
Changes in periodontal bleeding on probing BoP
Time frame: 12 months
Changes in periodontal plaque index PI
Time frame: 12 months
Subjective perception of discomfort and pain during surgery and the post-operative period
Time frame: 7 days
Analgesics taken
Time frame: 7 days
Treatment liking
Time frame: 7 days
Gingival color and texture appearance
Time frame: 12 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Sep 2023.
- Background: PubMed 6950834Abrams L. Augmentation of the deformed residual edentulous ridge for fixed prosthesis. Compend Contin Educ Gen Dent. 1980 May-Jun;1(3):205-13. No abstract available.
- Background: PubMed 27873018Bassetti RG, Stahli A, Bassetti MA, Sculean A. Soft tissue augmentation around osseointegrated and uncovered dental implants: a systematic review. Clin Oral Investig. 2017 Jan;21(1):53-70. doi: 10.1007/s00784-016-2007-9. Epub 2016 Nov 21.
- Background: PubMed 24210453El-Kholey KE. Efficacy and safety of a diode laser in second-stage implant surgery: a comparative study. Int J Oral Maxillofac Surg. 2014 May;43(5):633-8. doi: 10.1016/j.ijom.2013.10.003. Epub 2013 Nov 7.
- Background: PubMed 31860133Fons-Badal C, Alonso Perez-Barquero J, Martinez-Martinez N, Faus-Lopez J, Fons-Font A, Agustin-Panadero R. A novel, fully digital approach to quantifying volume gain after soft tissue graft surgery. A pilot study. J Clin Periodontol. 2020 May;47(5):614-620. doi: 10.1111/jcpe.13235. Epub 2020 Mar 12.
- Background: PubMed 24989333Fornaini C, Merigo E, Vescovi P, Bonanini M, Antonietti W, Leoci L, Lagori G, Meleti M. Different laser wavelengths comparison in the second-stage implant surgery: an ex vivo study. Lasers Med Sci. 2015 Aug;30(6):1631-9. doi: 10.1007/s10103-014-1623-3. Epub 2014 Jul 3.
- Background: PubMed 23826649Giannelli M, Formigli L, Bani D. Comparative evaluation of photoablative efficacy of erbium: yttrium-aluminium-garnet and diode laser for the treatment of gingival hyperpigmentation. A randomized split-mouth clinical trial. J Periodontol. 2014 Apr;85(4):554-61. doi: 10.1902/jop.2013.130219. Epub 2013 Jul 4.
- Background: PubMed 22834932Giannelli M, Formigli L, Lorenzini L, Bani D. Combined photoablative and photodynamic diode laser therapy as an adjunct to non-surgical periodontal treatment: a randomized split-mouth clinical trial. J Clin Periodontol. 2012 Oct;39(10):962-70. doi: 10.1111/j.1600-051X.2012.01925.x. Epub 2012 Jul 27.
- Background: PubMed 25171038Gonzalez-Martin O, Veltri M, Moraguez O, Belser UC. Quantitative three-dimensional methodology to assess volumetric and profilometric outcome of subepithelial connective tissue grafting at pontic sites: a prospective pilot study. Int J Periodontics Restorative Dent. 2014 Sep-Oct;34(5):673-9. doi: 10.11607/prd.1808.
- Background: PubMed 26660000Ozcelik O, Seydaoglu G, Haytac CM. Diode laser for harvesting de-epithelialized palatal graft in the treatment of gingival recession defects: a randomized clinical trial. J Clin Periodontol. 2016 Jan;43(1):63-71. doi: 10.1111/jcpe.12487. Epub 2016 Jan 21.
- Background: PubMed 22408781Park SH, Wang HL. Pouch roll technique for implant soft tissue augmentation: a variation of the modified roll technique. Int J Periodontics Restorative Dent. 2012 Jun;32(3):e116-21.
- Background: PubMed 33448379Parvini P, Galarraga-Vinueza ME, Obreja K, Magini RS, Sader R, Schwarz F. Prospective study assessing three-dimensional changes of mucosal healing following soft tissue augmentation using free gingival grafts. J Periodontol. 2021 Mar;92(3):400-408. doi: 10.1002/JPER.19-0640. Epub 2020 Aug 21.
- Background: PubMed 32143433Schmidt A, Klussmann L, Wostmann B, Schlenz MA. Accuracy of Digital and Conventional Full-Arch Impressions in Patients: An Update. J Clin Med. 2020 Mar 4;9(3):688. doi: 10.3390/jcm9030688.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Marco Giannelli, MD principal investigator
Odontostomatologic Laser Therapy Center
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Atrophy of Gingiva, run by Odontostomatologic Laser Therapy Center, Florence, Italy at 1 site in Italy.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 29 Sep 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Objectively measurable volume changes of the vestibular gingiva (time frame: 12 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06057363, which also lists 15 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Sep 2023; AzTrials last refreshed its copy on 6 Nov 2026.