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A clinical trial comparing cyanoacrylate and Fibrin Glue in the Treatment of Gum Recession.

Comparative Evaluation of Cyanoacrylate and Fibrin Glue in the Treatment of Gingival Recession- A Randomized control trial. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/07/113306
Enrollment
30
Registered
2026-07-03
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Health Condition 1: K060- Gingival recession

Interventions

Intervention1: Fibrin Sealant: Commercially available Fibrin sealant will be applied once intraoperatively during the surgical procedure. Patient will be followed at 14 days, 1 month and 3 months. Con

Sponsors

Ankita Dash
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Presence of Miller I or II gingival recession defects Good plaque control and oral hygiene

Exclusion criteria

Exclusion criteria: Smokers or tobacco users Patients with systemic disease affecting wound healing Pregnant or lactating women Allergies to components of cyanoacrylate or fibrin glue

Design outcomes

Primary

MeasureTime frame
Gingival Recession Depth and width Percentage of root coverageTimepoint: Baseline, 1 month and 3 months—

Secondary

MeasureTime frame
Probing depthTimepoint: Baseline, 1 month and 3 months;Clinical attachment levelTimepoint: Baseline, 1 month and 3 months;Width of Keratinized GingivaTimepoint: Baseline, 1 month and 3 months;Height of Keratinized GingivaTimepoint: Baseline, 1 month and 3 months—

Countries

India

Contacts

Public ContactAnkita Dash

Institute of Dental Sciences, Bhubaneswar

anuragsatpathy@soa.ac.in9338333999

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026