CompletedNot Applicable

m-VISTA Technique vs. CAF in the Treatment of Class III Multiple Recessions

Spain24 participantsStarted 2017-12-04

Plain-language summary

The main objective is to assess whether the percentage of root coverage (%RC) achieved in the treatment of multiples class III recessions using the technique we have called modified vestibular incision subperiosteal tunnel access (m-VISTA), which is a lateral approach subperiosteal tunnel technique, combined with a connective tissue graft is greater than that achieved through the coronally advance flap (CAF) technique together with a connective tissue graft.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients of the Master of Periodontology of the UPV / EHU. * Age ≥ 18 years. * Multiple recessions (more than two) Class III ≥ 2 mm deep, in which the interdental papilla does not extend beyond the cementoenamel line. * Absence of active periodontal disease. * Plaque index (O'Leary et al. 1972) and bleeding index (Ainamo and Bay 1975) ≤15%. * Informed consent. Exclusion Criteria: * Smokers \> 10 cigarettes / day. * Subjects with systemic conditions that contraindicate surgery. * Subjects that have taken analgesics and anti-inflammatory drugs in the last 72 hours. * Subjects taking opioids, anticonvulsants and antidepressants except serotonin selective inhibitors. * Women who are pregnant or nursing. * Patients who do not wish to participate in the study.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Percentage of root coverage (%CR)

Timeframe: 12 months

Trial details

NCT IDNCT03258996

SponsorAitziber Fernandez Jimenez

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2021-03-31

View on ClinicalTrials.gov More Gingival Recessions trials