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Covering the exposed gums using Chorion membrane by two different surgical techniques

Comparing treatment outcomes of modified VISTA in multiple adjacent gingival recession with chorion membrane - A randomized control trial. - mVISTA

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/07/020118
Enrollment
46
Registered
2019-07-09
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K056- Periodontal disease, unspecified

Interventions

Intervention1: Modified VISTA with chorion membrane.: Chorion membrane from cell tissue bank placed in the test groups. Control Intervention1: Modified VISTA with connective tissue graft.: Connective

Sponsors

Dr Marisca Austin Pereira
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Identifiable CEJ. 2. Age more than 18 years 3. Millerââ?¬•s class I and/or class II multiple adjacent gingival recession on the facial surface. 4. Patients who have given written informed consent after explanation of the surgical procedure.

Exclusion criteria

Exclusion criteria: 1. Subjects taking drugs known to interfere with periodontal wound healing. 2. Subjects who had received periodontal treatment in previous six months 3. Pregnant or lactating women 4. Patients with systemic disorders / conditions that are contraindicated for the periodontal surgical procedures. 5. Patients refusing to give their consent for the surgical procedures. 6. Dental malocclusion such as tooth/teeth rotations, teeth alignment out of arch.

Design outcomes

Primary

MeasureTime frame
To evaluate clinical root coverage, probing depth, clinical attachment level, width of keratinized tissue, gingival recession depth and gingival biotype obtained .Timepoint: Baseline (at the time of surgical procedure) and postoperative atleast 3 months

Secondary

MeasureTime frame
Patient comfort, complications such as hematoma, pain, swelling, etc.Timepoint: baseline and postoperative 3 months

Countries

India

Contacts

Public ContactDr Marisca Austin Pereira

Sinhgad Dental COllege and Hospital

dr_raghum2000@yahoo.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026