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Application of special pain relief patch(Buprenorphine) for patients undergoing key hole upper abdominal surgeries

Evaluation of analgesic efficacy of pre operative buprenorphine transdermal patch for acute post operative pain management in patients undergoing laparoscopic upper abdominal surgeries in a tertiary care hospital - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/07/091902
Enrollment
85
Registered
2025-07-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: K807- Calculus of gallbladder and bile duct without cholecystitis

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil Intervention4: Nil: Nil

Sponsors

nil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients aged 18 to 65 years. Patients scheduled for elective laparoscopic upper abdominal surgeries. Patients who are willing to give consent to participate in the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
To assess the efficacy of preoperative buprenorphine transdermal patch for acute post operative pain in patients undergoing upper abdominal laparoscopic surgeries Timepoint: post operative for first,second and third day—

Secondary

MeasureTime frame
nilTimepoint: nil—

Countries

India

Contacts

Public ContactDANDIBOYENA GANGA

sri siddartha institute of medical sciences

anitaprabhu16@gmail.com8095889575

Outcome results

None listed

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