MCAT Versus VISTA With Volume Stable Collagen Matrix in RT3 Gingival Recession (NCT06433986) | Clinical Trial Compass
UnknownNot Applicable
MCAT Versus VISTA With Volume Stable Collagen Matrix in RT3 Gingival Recession
India34 participantsStarted 2024-06-01
Plain-language summary
This study aims to compare MCAT technique (supraperiosteal approach with coronal advancement of flap) with VISTA technique(subperiosteal approach with coronal advancement of flap), Further, it may be hypothesized that supraperiosteal placement of graft material (in MCAT technique) may be better due to better blood supply, and MCAT technique utilizes a microsurgical concept, including microsurgical blades and suture material, which improves wound healing and establishes a better esthetic result and results in better outcome in terms of root coverage percentage compared to VISTA. Therefore, this study aims to compare minimally invasive technique MCAT and VISTA using VCMX as a graft in RT3 gingival recession in anterior teeth.
Who can participate
Age range
18 Years – 45 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 with RT 3 isolated recession defects present Labially in Anterior teeth region,with vestibular depth\>=6mm
* Systemically healthy individuals.
* Age \>18 years old.
* A full mouth plaque score (FMPS) and full mouth BOP (FMBOP) \< 20%
* Patient showing adequate compliance and willing to participate in the study.
EXCLUSION CRITERIA-
* Patients having systemic disease such as hypertension, diabetes, hyperthyroidism or on medication that influence the outcome of periodontal therapy.
* Previous surgical attempt to correct gingival recession.
* Crowding of affected teeth and tooth without adjacent contact teeth.
* Patients with active periodontal disease.
* Smokers and tobacco users.
* Pregnant and lactating women.
* Involved tooth with trauma from occlusion
* Involved tooth with prosthesis.
* Endodontically treated tooth.
* Tooth with cervical abrasion/undetectable CEJ/ caries.
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
1
Root coverage percentage
Timeframe: 6 months
Trial details
NCT IDNCT06433986
SponsorPostgraduate Institute of Dental Sciences Rohtak