Recession, GingivalNCT07143760
Topical Hyaluronic Acid Adjunctive Effects on Healing After Free Gingival Grafting in Smokers and Non-Smokers
An observational study of Recession, Gingival and Tissue Grafts, run by Istanbul University at 1 site in Turkey (Türkiye).
Trial summary
Comparison of the healing of free gingival grafts applied to smokers and non-smokers and evaluation of the effect of hyaluronic acid gel on healing of the donor site. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Recession, Gingival, Tissue Grafts
- What is being tested?
- Gengigel
- Type of treatment
- Medical device
- How many people
- 80 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 1 Jan 2018to 30 Nov 2022
- 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 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: After screening archived patient records from the Istanbul University, Dentistry Faculty, Department of Periodontology archive, a total of 80 patients who had undergone FGG surgery between January 2018 and November 2022 were deemed eligible and included in the study.
Who may be able to join
- Patients were eligible for inclusion if they were between 18 and 65 years of age, systemically healthy, and not taking regular medication. Additional criteria included the absence of antibiotic use within the last three months, no pregnancy or lactation, a periodontally healthy status or completion of periodontal therapy, and the presence of insufficient keratinised gingiva in the mandibular anterior region (canine-to-canine) with a clinical indication for FGG in the same area. Smoking and non-smoking status were determined from clinical records and patient self-reports. All smokers included in the study continued smoking throughout the documented postoperative period, and none of the non-smokers had a history of smoking or initiated smoking during the study period.
Who cannot join
- Subjects who do not meet these conditions will not be included in the study.
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Istanbul University, Dentistry Faculty, Department of Periodontology
Istanbul, 34116
About this study
Official title: Healing Response of Recipient and Donor Sites in Smokers and Non-Smokers Following Free Gingival Grafting: Adjunctive Effects of Topical Hyaluronic Acid on Palatal Healing
Comparison of the healing of free gingival grafts applied to smokers and non-smokers and evaluation of the effect of hyaluronic acid gel on healing of the donor site.
Read the detailed description
The oral mucosa consists of three main components: (1) masticatory mucosa, (2) specialized mucosa, and (3) lining mucosa. The masticatory mucosa is a keratinized tissue covering the gingiva and the hard palate. The gingiva itself can be classified into three distinct regions: (1) free gingiva, (2) interdental gingiva, and (3) attached gingiva. The free gingiva is composed of oral epithelium, oral sulcular epithelium, and junctional epithelium. Both the oral epithelium, interdental gingiva, and attached gingiva are keratinized tissues.
Keratinized gingiva can be histologically divided into the following cell layers based on the degree of keratin-producing cell differentiation:
Stratum basale (or stratum germinativum)
Stratum spinosum
Stratum granulosum
Stratum corneum
The absence of keratinized gingiva is classified under mucogingival deformities. These deformities represent deviations from the normal dimensional and morphological relationship between the gingiva and the alveolar mucosa and can often have negative esthetic and functional implications for patients. The lack of keratinized gingiva is addressed separately within mucogingival conditions.
In cases where patients present with a thin gingival biotype, inflammation and gingival recession can further reduce the protective capacity of the tissue, creating clinical scenarios in which mucogingival therapy should be considered. Lang and Löe suggested that an apico-coronal width of keratinized gingiva of less than 2 mm is insufficient to maintain gingival health. Today, the presence of attached gingiva is regarded as crucial for maintaining periodontal health. From a periodontal perspective, keratinized gingiva serves two primary functions:
Providing mechanical resistance against functional forces.
Offering a stable surface for toothbrushing, thus facilitating plaque control.
The 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions concluded that, although a minimum amount of keratinized tissue may not be required to prevent attachment loss when optimal plaque control is achieved, approximately 2 mm of keratinized tissue and 1 mm of attached gingiva around the teeth is considered necessary to maintain periodontal health.
The Free Gingival Graft (FGG) procedure, first described by Björn in 1963, is a surgical technique developed to increase the dimensions of keratinized tissue around teeth and prevent gingival recession. This method remains one of the most commonly employed approaches for augmenting keratinized gingiva. However, over time, transplanted tissue can undergo horizontal and vertical dimensional changes. This makes the long-term volumetric stability of keratinized gingiva after FGG procedures critical. Postoperative graft shrinkage is considered a clinical phenomenon that mainly occurs during the early healing phase.
During FGG surgery, a graft is harvested from the palatal donor site, which is then left to heal by secondary intention. The most frequently observed postoperative complications at the donor site include pain, burning sensation, delayed wound healing, and associated difficulties in eating. Over the years, various hemostatic agents, periodontal dressings, platelet-rich fibrin, and analgesics have been used to reduce these complications and support healing; however, no ideal material has been identified in the literature.
The mechanisms by which smoking affects periodontal status are not fully understood, but numerous potential pathways have been discussed in the literature, including effects on the oral microbiota, gingival tissues, inflammatory and immune responses, and the healing capacity of the periodontium. Although smoking does not directly influence plaque accumulation, it is widely accepted that it can impair various aspects of the innate immune response. In periodontitis, the balance between plaque and immune response may shift toward exaggerated tissue destruction, meaning that even a small amount of plaque can lead to disproportionate breakdown.
Evidence suggests that, in smokers, the function and adhesion of gingival and periodontal ligament fibroblasts may be compromised, collagenolytic activity may increase, and collagen production may decrease. Additionally, the suppression of gingival inflammation, reduction in bleeding on probing, and decreased gingival bleeding seen in smokers are not due to vasoconstriction of the gingival vasculature but rather to reduced angiogenesis within the tissues.
For these reasons, mucogingival problems are more prevalent among smokers, with a clear dose-response relationship. Smoking may also negatively impact both the short- and long-term success of periodontal plastic surgery procedures. As a result, the expected dimensions of keratinized gingiva at the recipient site may not be achieved, and smokers may face a higher risk of postoperative complications.
In a study smoking did not appear to have a noticeable impact on postoperative dimensional changes of FGG, it was shown to reduce postoperative bleeding and delay epithelialization, ultimately slowing donor site wound healing.
Hyaluronic acid (HA) is a high-molecular-weight, non-sulfated polysaccharide of the glycosaminoglycan family, found in various body fluids such as synovial fluid, serum, saliva, and gingival crevicular fluid. HA is present in all periodontal tissues-at higher concentrations in non-mineralized tissues like the gingiva and periodontal ligament and at lower levels in mineralized tissues like cementum and alveolar bone. HA is synthesized by mesenchymal cells such as fibroblasts, chondrocytes, and osteoblasts at the cell membrane.
Because HA is highly biocompatible and non-immunogenic, it has bacteriostatic, fungistatic, anti-inflammatory, anti-edematous, osteoinductive, and pro-angiogenic properties, contributing to wound healing in various tissues. These properties have made HA an attractive adjunct in fields such as orthopedics, ophthalmology, and dermatology for treating a range of conditions.
In dentistry, HA has been applied to accelerate healing in extraction sockets, treat temporomandibular joint osteoarthritis, maintain space in sinus lift procedures without grafting, and relieve pain associated with recurrent aphthous ulcers. In periodontology, HA has been proposed for use either as a monotherapy or as an adjunct to non-surgical and/or surgical periodontal therapy to reduce inflammation and support wound healing.
To the best of our knowledge, there is no study in the literature evaluating the potential effects of HA on VAS scores and healing outcomes specifically in smokers undergoing FGG surgery.
- Conditions
- Recession, Gingival, Tissue Grafts
- Being tested
- Gengigel
- Keywords
- free gingival graft, hyaluronic acid, smoking, visual analogue scale
- Medical subject headings
- Gingival Recession, Smoking
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
GengigelDevice
Free gingival graft (FGG) surgery leaves an open wound at the palatal donor site, which heals by secondary intention and can cause patient discomfort. Various adjunctive materials, such as stents, collagen sponges, platelet-rich fibrin, and hyaluronic acid (HA), have been explored to improve healing. HA is a naturally occurring glycosaminoglycan with hydrating, anti-inflammatory, and pro-regenerative properties that support fibroblast and keratinocyte activity and promote angiogenesis. These qualities make HA a promising adjunct for enhancing wound healing in periodontal surgery. However, few studies have assessed its clinical impact on palatal donor site healing after FGG, and in existing studies HA was applied only once by the operator rather than used consistently by patients. This study evaluates daily, patient-applied HA gel to address this gap and compare outcomes in smokers and non-smokers.
| Study group | Role | What they receive |
|---|---|---|
| Non-smokers who did not use Hyaluronic acid gel | This group consist subjects with Non-smokers who did not use Hyaluronic acid gel | |
| Non-smokers who used Hyaluronic acid gel | This group consist subjects with Non-smokers who used Hyaluronic acid gel Receives: Device: Gengigel | |
| Smokers who did not use Hyaluronic acid gel | This group consist subjects with Smokers who did not use Hyaluronic acid gel | |
| Smokers who used Hyaluronic acid gel | This group consist subjects with Smokers who used Hyaluronic acid gel Receives: Device: Gengigel |
What is being measured
The primary outcome is the main question the study is designed to answer.
Healing outcome of the palatal donor site
Clinical assessment of epithelialisation using standardised scoring. Assessment of the palatal donor site was undertaken through standardised measurements of graft epithelialisation at predefined intervals using a Williams periodontal probe.
Measured: Baseline, Day 7 , Day 14, 1. Month, 3. Months
Secondary outcomes (1)
Visual Analogue Scale pain scores
Patient-reported pain levels measured using a 10-cm visual analogue scale.
Measured: Days 3, 7, 10, and 14 postoperatively
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Aug 2025
- Study start1 Jan 2018
- Primary completion30 Nov 2022
- Study completion30 Nov 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (5)Papers the sponsor has linked to this study.
- Other trials for Recession, GingivalStudies of the same condition, open and under way.
- More trials run by Istanbul UniversityThe sponsor's other registered studies.
- 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
- Retrospective
- Enrolment
- 80 participants (actual)
Sponsor and investigators
- Lead sponsor
- Istanbul University
- Sponsor type
- University, hospital or other
- Collaborators
- Ricerfarma S.r.l
- Responsible party
- Principal investigator, Emine Çifcibaşı, Istanbul University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07143760
- Sponsor's protocol ID
- 2023/18
- Status last verified
- Aug 2025
- First submitted
- 6 Aug 2025
- Last updated
- 27 Aug 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- Yes
- Individual data sharing
- No
Publications
Yildirim S, Ozener HO, Dogan B, Kuru B. Effect of topically applied hyaluronic acid on pain and palatal epithelial wound healing: An examiner-masked, randomized, controlled clinical trial. J Periodontol. 2018 Jan;89(1):36-45. doi: 10.1902/jop.2017.170105.
PubMed 28914592Silva CO, Ribeiro Edel P, Sallum AW, Tatakis DN. Free gingival grafts: graft shrinkage and donor-site healing in smokers and non-smokers. J Periodontol. 2010 May;81(5):692-701. doi: 10.1902/jop.2010.090381.
PubMed 20429648Hatipoglu H, Keceli HG, Guncu GN, Sengun D, Tozum TF. Vertical and horizontal dimensional evaluation of free gingival grafts in the anterior mandible: a case report series. Clin Oral Investig. 2007 Jun;11(2):107-13. doi: 10.1007/s00784-006-0084-x. Epub 2007 Feb 9.
PubMed 17294229Cifcibasi E, Karabey V, Koyuncuoglu C, Duzagac E, Genceli E, Kasali K, Cintan S. Clinical evaluation of free gingival graft shrinkage in horizontal and vertical dimensions. J Istanb Univ Fac Dent. 2015 Oct 21;49(3):11-16. doi: 10.17096/jiufd.58759. eCollection 2015.
PubMed 28955540Björn, H. (1963). Free Transplantation of Gingiva Propria. Odontol. Rev.
Study at a glance
From the registry record, last updated by the sponsor on 27 Aug 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Healing Response of Recipient and Donor Sites in Smokers and Non-Smokers Following Free Gingival Grafting: Adjunctive Effects of Topical Hyaluronic Acid on Palatal Healing
- ClinicalTrials.gov ID
- NCT07143760
- Acronym / sponsor ID
- 2023/18
- Conditions
- Recession, Gingival, Tissue Grafts
- Keywords
- free gingival graft, hyaluronic acid, smoking, visual analogue scale
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 80 participants (actual)
- Lead sponsor
- Istanbul UniversityUniversity, hospital or other
- Collaborators
- Ricerfarma S.r.l
- Study start
- 1 Jan 2018 (actual)
- Primary completion
- 30 Nov 2022 (actual)
- Study completion
- 30 Nov 2022 (actual)
- First posted
- 27 Aug 2025 (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.
Comparison of the healing of free gingival grafts applied to smokers and non-smokers and evaluation of the effect of hyaluronic acid gel on healing of the donor site.
Detailed description
The oral mucosa consists of three main components: (1) masticatory mucosa, (2) specialized mucosa, and (3) lining mucosa. The masticatory mucosa is a keratinized tissue covering the gingiva and the hard palate. The gingiva itself can be classified into three distinct regions: (1) free gingiva, (2) interdental gingiva, and (3) attached gingiva. The free gingiva is composed of oral epithelium, oral sulcular epithelium, and junctional epithelium. Both the oral epithelium, interdental gingiva, and attached gingiva are keratinized tissues.
Keratinized gingiva can be histologically divided into the following cell layers based on the degree of keratin-producing cell differentiation:
Stratum basale (or stratum germinativum)
Stratum spinosum
Stratum granulosum
Stratum corneum
The absence of keratinized gingiva is classified under mucogingival deformities. These deformities represent deviations from the normal dimensional and morphological relationship between the gingiva and the alveolar mucosa and can often have negative esthetic and functional implications for patients. The lack of keratinized gingiva is addressed separately within mucogingival conditions.
In cases where patients present with a thin gingival biotype, inflammation and gingival recession can further reduce the protective capacity of the tissue, creating clinical scenarios in which mucogingival therapy should be considered. Lang and Löe suggested that an apico-coronal width of keratinized gingiva of less than 2 mm is insufficient to maintain gingival health. Today, the presence of attached gingiva is regarded as crucial for maintaining periodontal health. From a periodontal perspective, keratinized gingiva serves two primary functions:
Providing mechanical resistance against functional forces.
Offering a stable surface for toothbrushing, thus facilitating plaque control.
The 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions concluded that, although a minimum amount of keratinized tissue may not be required to prevent attachment loss when optimal plaque control is achieved, approximately 2 mm of keratinized tissue and 1 mm of attached gingiva around the teeth is considered necessary to maintain periodontal health.
The Free Gingival Graft (FGG) procedure, first described by Björn in 1963, is a surgical technique developed to increase the dimensions of keratinized tissue around teeth and prevent gingival recession. This method remains one of the most commonly employed approaches for augmenting keratinized gingiva. However, over time, transplanted tissue can undergo horizontal and vertical dimensional changes. This makes the long-term volumetric stability of keratinized gingiva after FGG procedures critical. Postoperative graft shrinkage is considered a clinical phenomenon that mainly occurs during the early healing phase.
During FGG surgery, a graft is harvested from the palatal donor site, which is then left to heal by secondary intention. The most frequently observed postoperative complications at the donor site include pain, burning sensation, delayed wound healing, and associated difficulties in eating. Over the years, various hemostatic agents, periodontal dressings, platelet-rich fibrin, and analgesics have been used to reduce these complications and support healing; however, no ideal material has been identified in the literature.
The mechanisms by which smoking affects periodontal status are not fully understood, but numerous potential pathways have been discussed in the literature, including effects on the oral microbiota, gingival tissues, inflammatory and immune responses, and the healing capacity of the periodontium. Although smoking does not directly influence plaque accumulation, it is widely accepted that it can impair various aspects of the innate immune response. In periodontitis, the balance between plaque and immune response may shift toward exaggerated tissue destruction, meaning that even a small amount of plaque can lead to disproportionate breakdown.
Evidence suggests that, in smokers, the function and adhesion of gingival and periodontal ligament fibroblasts may be compromised, collagenolytic activity may increase, and collagen production may decrease. Additionally, the suppression of gingival inflammation, reduction in bleeding on probing, and decreased gingival bleeding seen in smokers are not due to vasoconstriction of the gingival vasculature but rather to reduced angiogenesis within the tissues.
For these reasons, mucogingival problems are more prevalent among smokers, with a clear dose-response relationship. Smoking may also negatively impact both the short- and long-term success of periodontal plastic surgery procedures. As a result, the expected dimensions of keratinized gingiva at the recipient site may not be achieved, and smokers may face a higher risk of postoperative complications.
In a study smoking did not appear to have a noticeable impact on postoperative dimensional changes of FGG, it was shown to reduce postoperative bleeding and delay epithelialization, ultimately slowing donor site wound healing.
Hyaluronic acid (HA) is a high-molecular-weight, non-sulfated polysaccharide of the glycosaminoglycan family, found in various body fluids such as synovial fluid, serum, saliva, and gingival crevicular fluid. HA is present in all periodontal tissues-at higher concentrations in non-mineralized tissues like the gingiva and periodontal ligament and at lower levels in mineralized tissues like cementum and alveolar bone. HA is synthesized by mesenchymal cells such as fibroblasts, chondrocytes, and osteoblasts at the cell membrane.
Because HA is highly biocompatible and non-immunogenic, it has bacteriostatic, fungistatic, anti-inflammatory, anti-edematous, osteoinductive, and pro-angiogenic properties, contributing to wound healing in various tissues. These properties have made HA an attractive adjunct in fields such as orthopedics, ophthalmology, and dermatology for treating a range of conditions.
In dentistry, HA has been applied to accelerate healing in extraction sockets, treat temporomandibular joint osteoarthritis, maintain space in sinus lift procedures without grafting, and relieve pain associated with recurrent aphthous ulcers. In periodontology, HA has been proposed for use either as a monotherapy or as an adjunct to non-surgical and/or surgical periodontal therapy to reduce inflammation and support wound healing.
To the best of our knowledge, there is no study in the literature evaluating the potential effects of HA on VAS scores and healing outcomes specifically in smokers undergoing FGG surgery.
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| Non-smokers who did not use Hyaluronic acid gel | – | –This group consist subjects with Non-smokers who did not use Hyaluronic acid gel |
| Non-smokers who used Hyaluronic acid gel | – | Device: GengigelThis group consist subjects with Non-smokers who used Hyaluronic acid gel |
| Smokers who did not use Hyaluronic acid gel | – | –This group consist subjects with Smokers who did not use Hyaluronic acid gel |
| Smokers who used Hyaluronic acid gel | – | Device: GengigelThis group consist subjects with Smokers who used Hyaluronic acid gel |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- After screening archived patient records from the Istanbul University, Dentistry Faculty, Department of Periodontology archive, a total of 80 patients who had undergone FGG surgery between January 2018 and November 2022 were deemed eligible and included in the study.
Key inclusion criteria (1 listed)
- Patients were eligible for inclusion if they were between 18 and 65 years of age, systemically healthy, and not taking regular medication. Additional criteria included the absence of antibiotic use within the last three months, no pregnancy or lactation, a periodontally healthy status or completion of periodontal therapy, and the presence of insufficient keratinised gingiva in the mandibular anterior region (canine-to-canine) with a clinical indication for FGG in the same area. Smoking and non-smoking status were determined from clinical records and patient self-reports. All smokers included in the study continued smoking throughout the documented postoperative period, and none of the non-smokers had a history of smoking or initiated smoking during the study period.
Key exclusion criteria (1 listed)
- Subjects who do not meet these conditions will not be included in the study.
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 |
|---|---|---|
| GengigelFree gingival graft (FGG) surgery leaves an open wound at the palatal donor site, which heals by secondary intention and can cause patient discomfort. Various adjunctive materials, such as stents, collagen sponges, platelet-rich fibrin, and hyaluronic acid (HA), have been explored to improve healing. HA is a naturally occurring glycosaminoglycan with hydrating, anti-inflammatory, and pro-regenerative properties that support fibroblast and keratinocyte activity and promote angiogenesis. These qualities make HA a promising adjunct for enhancing wound healing in periodontal surgery. However, few studies have assessed its clinical impact on palatal donor site healing after FGG, and in existing studies HA was applied only once by the operator rather than used consistently by patients. This study evaluates daily, patient-applied HA gel to address this gap and compare outcomes in smokers and non-smokers. | Device | Non-smokers who used Hyaluronic acid gel, Smokers who used Hyaluronic acid gel |
Primary outcome
Healing outcome of the palatal donor site
Time frame: Baseline, Day 7 , Day 14, 1. Month, 3. Months
Clinical assessment of epithelialisation using standardised scoring. Assessment of the palatal donor site was undertaken through standardised measurements of graft epithelialisation at predefined intervals using a Williams periodontal probe.
1 secondary outcome
Visual Analogue Scale pain scores
Time frame: Days 3, 7, 10, and 14 postoperatively
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 27 Aug 2025.
- Background: PubMed 28914592Yildirim S, Ozener HO, Dogan B, Kuru B. Effect of topically applied hyaluronic acid on pain and palatal epithelial wound healing: An examiner-masked, randomized, controlled clinical trial. J Periodontol. 2018 Jan;89(1):36-45. doi: 10.1902/jop.2017.170105.
- Background: PubMed 20429648Silva CO, Ribeiro Edel P, Sallum AW, Tatakis DN. Free gingival grafts: graft shrinkage and donor-site healing in smokers and non-smokers. J Periodontol. 2010 May;81(5):692-701. doi: 10.1902/jop.2010.090381.
- Background: PubMed 17294229Hatipoglu H, Keceli HG, Guncu GN, Sengun D, Tozum TF. Vertical and horizontal dimensional evaluation of free gingival grafts in the anterior mandible: a case report series. Clin Oral Investig. 2007 Jun;11(2):107-13. doi: 10.1007/s00784-006-0084-x. Epub 2007 Feb 9.
- Background: PubMed 28955540Cifcibasi E, Karabey V, Koyuncuoglu C, Duzagac E, Genceli E, Kasali K, Cintan S. Clinical evaluation of free gingival graft shrinkage in horizontal and vertical dimensions. J Istanb Univ Fac Dent. 2015 Oct 21;49(3):11-16. doi: 10.17096/jiufd.58759. eCollection 2015.
- BackgroundBjörn, H. (1963). Free Transplantation of Gingiva Propria. Odontol. Rev.
- 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.
The record lists no contact. Use the official record to reach the sponsor.
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 Recession, Gingival and Tissue Grafts, run by Istanbul University at 1 site in Turkey (Türkiye).
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 1 inclusion and 1 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 27 Aug 2025. 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 Turkey (Türkiye). 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?
Healing outcome of the palatal donor site (time frame: Baseline, Day 7 , Day 14, 1. Month, 3. Months). 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 NCT07143760, which also lists 5 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 27 Aug 2025.