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Efficacy evaluation of Methadone vs Fentanyl for neuropathic pain in head and neck cancers

Comparing the analgesic efficacy of Methadone and Fentanyl for neuropathic pain in patients of head and neck cancers: A Equivalent Randomised Controlled Trial - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079730
Enrollment
110
Registered
2025-01-29
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: C00-C14- Malignant neoplasms of lip, oral cavity and pharynx

Interventions

Intervention1: Evaluation of efficacy of Methadone for neuropathic pain in patients of head and neck malignancy.: Analgesic optimisation with methadone syrup for relief of neuropathic pain head and ne

Sponsors

Dr BRA IRCH, All India Institute of Medical Sciences,New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age greater than 18 years and less than 65 years. Patients with head and neck malignancy having neuropathic pain who have corrected QT interval Patients who are already on stronger opioids for more than 14 days and still have pain score more than 4 on NRS.

Exclusion criteria

Exclusion criteria: Patients who have received tablet morphine for less than 2 weeks or on weaker opioids. Patients with deranged renal functions, dyselectrolytemia and abnormal ECG. Patients currently in fever. Patients not willing to apply transdermal patch.

Design outcomes

Primary

MeasureTime frame
To compare the analgesic efficacy of Methadone and Fentanyl for neuropathic pain in head and neck malignancies.Timepoint: Patient will be evaluated at 1 week, 3 week, 5 week, 2 months and 3 months.

Secondary

MeasureTime frame
To evaluate reduction in pain after 1 week, 3 week, 5 week, 2 months and 3 months. To determine the breakthrough pain with the given medications.Timepoint: Patient will be evaluated at 1 week, 3 week, 5 week, 2 months and 3 months.

Countries

India

Contacts

Public ContactDr Sachidanand Jee Bharati

All India Institute of Medical Sciences, New Delhi

sachidadr@yahoo.co.in9968436042

Outcome results

None listed

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