FindTrial
Sign In

Comparison of pain relief in patients undergoing spine surgery between Buprenorphine patch and Intravenous Tramadol

COMPARISON OF POSTOPERATIVE PAIN RELIEF WITH BUPRENORPHINE TRANSDERMAL PATCH VERSUS INTRAVENOUS TRAMADOL IN ADULT PATIENTS UNDERGOING SPINE SURGERIES.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/053532
Enrollment
100
Registered
2023-06-05
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Health Condition 1: M968- Other intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified

Interventions

Intervention1: Buprenorphine transdermal patch: Buprenorphine transdermal patch 10mcg/hr will be applied on clean hairless skin 12 hours before surgery and kept for 48hours after surgery Control Inter

Sponsors

VMMC AND SAFDARJUNG HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients aged 18-60 years belonging to American society of anaesthesiology physical status (ASA) grade I & II undergoing elective spinal surgery.

Exclusion criteria

Exclusion criteria: Any known history of allergy to buprenorphine, pregnancy and lactation, Patients on antidepressants, on opioid therapy, opioid dependant or sensitive patients

Design outcomes

Primary

MeasureTime frame
To assess Total dose of rescue analgesics requiredTimepoint: 24hr, 48hr post surgery—

Secondary

MeasureTime frame
To assess: VAS score Hemodynamic parameters: Heart rate, systolic, diastolic and mean arterial Pressure Time of first rescue analgesic requirementTimepoint: 30min, 2hr, 4hr, 6hr, 12hr, 24hr—

Countries

India

Contacts

Public ContactDr Rajpal Singh

VMMC AND SAFDARJUNG HOSPITAL

doctorrajpal04@gmail.com9911858311

Outcome results

None listed

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