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A future study involving observation aimed to assess pain occurring after surgery at the surgical sites in head and neck cancer patients who were undergoing cosmetic surgery.

Postoperative donor site pain in head and neck cancer patients following reconstructive free tissue transfer surgery: A Prospective Observational Study - NIL

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/04/065069
Enrollment
250
Registered
2024-04-02
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: C068- Malignant neoplasm of overlappingsites of other and unspecified parts of mouth Health Condition 2: O- Medical and Surgical

Interventions

Sponsors

Tata Memorial Hospital
Lead Sponsor
Not Any
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: All adults age more than 18 years patients undergoing head and neck surgery with free flap reconstruction.

Exclusion criteria

Exclusion criteria: 3 Age less than 18 years 2 Patients requiring prolonged post-operative ventilator support more than 2 days 1 Pregnant and Lactating women

Design outcomes

Primary

MeasureTime frame
Incidence and severity of donor site pain in the postoperative periodTimepoint: up to day 5 after enrollment

Secondary

MeasureTime frame
1 Nature of pain Somatic or neuropathic based on patients descriptionTimepoint: up to day 5 after enrollment;2 Incidence of Neuropathic painTimepoint: up to day 5 after enrollment;3 Duration of analgesics used in the postoperative periodTimepoint: up to day 5 after enrollment;4 Need for Acute Pain Services referralTimepoint: up to day 5 after enrollment

Countries

India

Contacts

Public ContactKomal Nikhare

Tata Memorial Hospital,Mumbai

vandanachaukar@hotmail.com9819762668

Outcome results

None listed

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