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Comparative Study Between Radial Forearm Free Flap[RAFF] And Pectoralis Major Myocutaneous Pedicle Flap[PMMF] In Maxillofacial Oncologic Surgical Defects A RANDOMISED CONTROL TRIAL

Comparision of Radial Forearm Free Flap and Pectoralis Major Myocutaneous Pedicle Flap in maxillofacial oncologiacl defect in view of esthetics, functional outcome,feeding tube dependency ,mouth opening and quality of life post surgery A randomised control - NILL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101156
Enrollment
36
Registered
2026-01-14
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Health Condition 1: C148- Malignant neoplasm of overlappingsites of lip, oral cavity and pharynx

Interventions

Intervention1: radial fore-arm flap reconstruction as intervention marked as group A and Pectoralis Major Myocutaneous Flap reconstruction as comparator group named as group B: Participants will under

Sponsors

SIKSHA O ANUSANDHAN
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: patient with oral squamous cell carcinoma proven by biopsy, planned for single stage resection and soft tissue flap reconstruction

Exclusion criteria

Exclusion criteria: -Patients not available for complete follow-up during the postoperative assessment period. -Patients with collagen disorders and haematological disorders. -Negative Allens test (for case of RFAFF cases only) -Patients with history of previous surgery, radiation or chemotherapy in head and neck region.

Design outcomes

Primary

MeasureTime frame
to examine donor site complications ,esthetics and functional outcome and quality of lifeTimepoint: 1 month,3 month and 6 month post operatively—

Secondary

MeasureTime frame
Functional outcomes -Speech (using an assessment scale) -Swallowing (Mann Assessment of Swallowing Ability Oral Cancer [MASA-C]) -Feeding tube dependence Esthetic outcome (measured by POSAS Patient Scale) Donor site complications (POSAS Observer Scale)Timepoint: 30 days,60days,90 days—

Countries

India

Contacts

Public ContactDr Upasa Sarma Medhi

INSTITUTE OF DENTAL SCIENCES, SIKSHA O ANUSANDHAN

subratpadhiary@soa.ac.in7086046827

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026