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Collagen membrane study

A prospective audit of functional outcomes after using collagen membrane for intraoral mucosal defects. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/02/104654
Enrollment
30
Registered
2026-02-24
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: C069- Malignant neoplasm of mouth, unspecified

Interventions

Intervention1: collagen membrane: Collagen-based wound dressings have long been used to cover burn wounds and treat ulcers. Collagen dressings have been prepared with a semi-occlusive polymer film at

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion Criteria: 1.Buccal mucosa lesions planned for peroral excision, amenable for closure using collagen membrane. 2.Age above 18 years, willing to give valid consent

Exclusion criteria

Exclusion criteria: Exclusion Criteria: 1.Lesions requiring skin or bone resection. 2. Lesions requiring cheek flap raising or flap reconstruction(local /distant) 3. Severe OSMF

Design outcomes

Primary

MeasureTime frame
To assess efficacy of a collagen membrane (time taken for complete mucosalisation of defect) as a graft in healing of intraoral surgical defects.Timepoint: 1 month—

Secondary

MeasureTime frame
Effect of collagen membrane application on post-surgery mouth opening.Timepoint: 1 month—

Countries

India

Contacts

Public ContactDr Vidisha Tuljapurkar

Tata Memorial Hospital

vidishavt@yahoo.com24177000

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026