AzTrials
AzTrials

Root Canal TreatmentNCT05374434

A First in Human Study to Compare Feasibility of Inertial Cavitation Irrigation to SNI in Root Canal Treatment.

A study testing Conventional irrigation and Inertial cavitation in people with Root Canal Treatment and Post Operative Pain, run by Lumendo AG at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The study design is a single-center 2-arm randomized controlled clinical trial. 10 subjects (teeth) requiring a root canal treatment will be enrolled in 2 groups (5 in each group). Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Root Canal Treatment, Post Operative Pain
What is being tested?
Conventional irrigation and Inertial cavitation
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
10 participants
Where
1 siteTurkey (Türkiye)
Study dates
10 May 2022to 31 May 2022
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

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 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Physical status classification system described was used for patients' recruitment. Healthy patients, who were classified by the American Society of Anaesthesiologists (ASA) as ASA I and II
  • Patients with the age of 18 and over
  • Patients who were diagnosed as in need of non-surgical orthograde root canal treatment of an asymptomatic tooth
  • Tooth without signs of previously initiated Root Canal Therapy

Who cannot join

  • Pregnant and lactating females
  • Patients with chronic periodontal diseases
  • Patients with sensitivity or adverse reactions to any medication or materials that were used throughout the treatment procedure
  • Patients with acute periapical periodontitis
  • Patients with acute periodontal abscess
  • Patients who could not abide by the follow-up time
Show all 17Show fewer
  • Patients who used analgesics 1-week prior or antibiotics 1-month prior to treatment
  • Uncooperative patients
  • Teeth that cannot be made functional nor restored or difficult to access teeth with no importance (wisdom teeth)
  • Teeth with poor prognosis, for example, due to deep root caries or big root resorption
  • Teeth with more than/or equal 4 mm periodontal pocket depth
  • Teeth with an inaccessible root end
  • Teeth with apical resorption or a radiologically not clearly defined apex
  • Fractured teeth
  • Teeth with immature or open apices
  • Teeth with root apices extending into the maxillary sinus
  • Teeth with external resorption communicating with the pulp

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • İstanbul Medipol Universitesi, Faculty of Dentistry, Department of Endodontics

    Istanbul, Unkapanı, Fatih, 34083

Other trials in Turkey (Türkiye)

About this study

Official title: Comparative Evaluation of the Effectiveness of Root Canal Preparation After Irrigation Using Endodontic Needle and Inertial Cavitation: A Randomized Controlled Trial

The study design is a single-center 2-arm randomized controlled clinical trial. 10 subjects (teeth) requiring a root canal treatment will be enrolled in 2 groups (5 in each group). The aim of the study is to compare the postoperative pain intensity levels in patients with asymptomatic teeth diagnosed for non-surgical orthograde root canal treatment that are disinfected during the root canal treatment procedure by manual irrigation with sodium hypochlorite (NaOCl) solution using an endodontic needle or by a inertial cavitation-generating device.

Read the detailed description

Inclusion Criteria:

  1. Physical status classification system described was used for patients' recruitment. Healthy patients, who were classified by the American Society of Anaesthesiologists (ASA) as ASA I and II
  2. Patients with the age of 18 and over
  3. Patients who were diagnosed as in need of non-surgical orthograde root canal treatment of an asymptomatic tooth
  4. Tooth without signs of previously initiated Root Canal Therapy

Exclusion Criteria:

  1. Pregnant and lactating females
  2. Patients with chronic periodontal diseases
  3. Patients with sensitivity or adverse reactions to any medication or materials that were used throughout the treatment procedure
  4. Patients with acute periapical periodontitis
  5. Patients with acute periodontal abscess
  6. Patients who could not abide by the follow-up time
  7. Patients who used analgesics 1-week prior or antibiotics 1-month prior to treatment
  8. Uncooperative patients
  9. Teeth that cannot be made functional nor restored or difficult to access teeth with no importance (wisdom teeth)
  10. Teeth with poor prognosis, for example, due to deep root caries or big root resorption
  11. Teeth with 4 mm periodontal pocket depth
  12. Teeth with an inaccessible root end
  13. Teeth with apical resorption or a radiologically not clearly defined apex
  14. Fractured teeth
  15. Teeth with immature or open apices Confidential
  16. Teeth with root apices extending into the maxillary sinus

All treatment procedures will be performed in a single visit by a single treatment provider. It will be assured that the operation room is quiet and isolated throughout the whole process to avoid any outside interference. Patients will be made comfortable and informed about the steps of the procedure a second time right before commencing the treatment protocol. Patients will be also reminded that they will get the necessary treatment even if they decline from the study and should not feel compelled to participate the study for a proper treatment. All root canal treatments will be performed using a dental loupe with a magnification of 4.50X (EyeMag Pro F; Carl Zeiss).

Each tooth will be anaesthetized with 2 mL local anaesthetic solution containing 40 mg/mL articaine hydrochloride and 12 mg/mL epinephrine hydrochloride (Ultracaine DS Forte; Aventis Pharma). After isolating the tooth with a rubber dam (Hygenic Dental Dam Kit; Coltene/Whaledent Gmbh \& Co.kg, Langenau, Germany) the operation field will be disinfected using 5.25% NaOCl solution (Wizard; Rehber Chemistry) soaked cotton rolls. After the access cavity preparation, a #10 C-File (MMC file, Coltene-Micro-Méga, Besançon, France) will be introduced into the root canal for scouting. Coronal flaring of root canals will be performed using a nickel-titanium flaring file (One Flare; Coltene-Micro-Méga) with an electric endodontic motor (Dual Move, Coltene-Micromega). Working length determination will be performed with a #10 C-file (MMC file, Coltene-Micro-Méga) and glidepath preparation will be completed with a One G (Coltene-Micro-Méga). The shaping of the root canals will be performed using One Curve (#25/0.06, Coltene-Micro-Méga). If further shaping of the canal will be needed 2 Shape F35 (#35/0.06) (ColteneMicro-Méga) files will be used according to apical canal lumen. All rotary files will be used according to the manufacturer's instructions. The filing protocols and files used will be recorded in the patient file.

In Group 1, 2 mL of NaOCl solution will be used after each file as an irrigation solution. After the shaping of the root canal is completed final irrigation with a 31G double side vented tip is performed in each canal using 2.5 mL of 5% EDTA (Wizard; Rehber Chemistry) for 1 minute, 2.5 mL of 5.25% NaOCl for 30 seconds and 5 mL of saline solution for 30 seconds respectively.

In Group 2, 2 mL of NaOCl solution will be used after each file as an irrigation solution. After the shaping of the root canal is completed, the NaOCl solution is removed from the root canal with 2.5 mL saline solution using a syringe with a 31G needle. EndoClean tip is introduced into the root canal, always maintaining a distance of at least 3mm from the apex. The EndoClean device is used for 60 seconds for each root canal.

In both groups, following root canal preparation, a matching gutta-percha cone (#25/0.06 or #35/0.06) (MM GP Points, Coltene-Micro-Méga) is introduced into the root canal coated with a calcium silicate-based root canal sealer (BioRoot RCS; Lancester PA, USA). Single-cone technique is used to fill the root canals.

Total-etch technique is used to restore the coronal part of each tooth. The cavities are etched with 35% H3PO4 for 15 seconds before a single layer application of an adhesive material (Adper Single Bond 2; 3M ESPE). After photopolymerization (Elipar S10, 3M ESPE) of the adhesive material for 20 seconds, a flowable bulk-fill composite material (Estelite, BulkFill Flow, Tokuyama Dental, Tokyo, Japan) is used to restore the coronal cavity incrementally with a thickness of 4 mm for every layer. Each layer is photopolymerized for 20 seconds.

Post-endodontic pain assessment :

After the treatment, all participants will be provided with analgesics (75 mg diclofenac sodium) (Voltaren SR 75 mg, Novartis, Kurtköy, İstanbul) and will be advised to use them if needs be and record the time of use. A pain intensity evaluation diary including VAS diagrams with their respective follow-up evaluation times will be provided to each participant to mark their pain. All participants will be contacted on their follow-up time to remind them to mark their pain intensity scores. Pain intensity of patients will be evaluated at 6h, 24h, 48h, 72h and 1 week after the completion of root canal treatment as previously described. Any complication such as paraesthesia, acute exacerbations, flare-ups, swellings will be also recorded on patients' charts. Patients who fail to abide by the followup time will be traced via phone, e-mail or SMS to determine the possible reasons for dropout.

Being tested
Conventional irrigation, Inertial cavitation
Keywords
Root Canal Irrigation, Root Canal Cleaning, Root Canal Treatment, Post Operative Pain, Root Canal Disinfection, Inertial cavitation, NaOCl Irrigation, Debridement
Medical subject headings
Pain, Postoperative

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Conventional irrigationOther

    The participant will be treated by manual irrigation with sodium hypochlorite NaOCl.

  • Inertial cavitationDevice

    The participant will be treated by inertial cavitation-generating device, that generates hydraulic cavitation to clean root canals deeper and more effectively than other existing systems.

Study groups in NCT05374434
Study groupRoleWhat they receive
Conventional irrigationActive comparatorRoot canal cleaning will be performed by manual irrigation with sodium hypochlorite NaOCl solution.
Receives: Other: Conventional irrigation
Inertial cavitationExperimentalRoot canal cleaning will be performed by inertial cavitation-generating device.
Receives: Device: Inertial cavitation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Clinical Postoperative Pain

    Pain intensity levels were graded using Visual Analog Scale (VAS). This scale is a horizontal 100 mm bar, marked in every 10mm with two ends. One end (0) indicated "no pain" and the other end (100) indicated "worst pain possible". Categorization of pain scores is as follows: 0-4 mm = No Pain, 5-44 mm = Mild Pain, 45-74 mm = Moderate Pain, 75-100 mm = severe pain.

    Measured: 6 hours

  2. Clinical Postoperative Pain

    Pain intensity levels were graded using Visual Analog Scale (VAS). This scale is a horizontal 100 mm bar, marked in every 10mm with two ends. One end (0) indicated "no pain" and the other end (100) indicated "worst pain possible". Categorization of pain scores is as follows: 0-4 mm = No Pain, 5-44 mm = Mild Pain, 45-74 mm = Moderate Pain, 75-100 mm = severe pain.

    Measured: 24 hours

  3. Clinical Postoperative Pain

    Pain intensity levels were graded using Visual Analog Scale (VAS). This scale is a horizontal 100 mm bar, marked in every 10mm with two ends. One end (0) indicated "no pain" and the other end (100) indicated "worst pain possible". Categorization of pain scores is as follows: 0-4 mm = No Pain, 5-44 mm = Mild Pain, 45-74 mm = Moderate Pain, 75-100 mm = severe pain.

    Measured: 48 hours

  4. Clinical Postoperative Pain

    Pain intensity levels were graded using Visual Analog Scale (VAS). This scale is a horizontal 100 mm bar, marked in every 10mm with two ends. One end (0) indicated "no pain" and the other end (100) indicated "worst pain possible". Categorization of pain scores is as follows: 0-4 mm = No Pain, 5-44 mm = Mild Pain, 45-74 mm = Moderate Pain, 75-100 mm = severe pain.

    Measured: 72 hours

  5. Clinical Postoperative Pain

    Pain intensity levels were graded using Visual Analog Scale (VAS). This scale is a horizontal 100 mm bar, marked in every 10mm with two ends. One end (0) indicated "no pain" and the other end (100) indicated "worst pain possible". Categorization of pain scores is as follows: 0-4 mm = No Pain, 5-44 mm = Mild Pain, 45-74 mm = Moderate Pain, 75-100 mm = severe pain.

    Measured: 1 week

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 May 2022
  2. Study start10 May 2022
  3. Primary completion31 May 2022
  4. Study completion31 May 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Device feasibility
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
10 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05374434
Sponsor's protocol ID
LUM-EC-001-060522
Status last verified
Jul 2024
First submitted
10 May 2022
Last updated
25 Jul 2024
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Conventional irrigation and Inertial cavitation in people with Root Canal Treatment and Post Operative Pain, run by Lumendo AG 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 4 inclusion and 17 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 25 Jul 2024. 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?

Yes. Results are posted in the registry (first posted 25 Jul 2024). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

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?

Clinical Postoperative Pain (time frame: 6 hours). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 25 Jul 2024.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in