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Effect of Preoperative Low dose Transdermal Buprenorphine patch on Spinal anesthesia - a Randomized control study

Effect of Preoperative Low dose Transdermal Buprenorphine patch(5mg) on spinal anesthesia- a Randomized control study - Transdermal Buprenorphine Patch effect

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/09/036324
Enrollment
84
Registered
2021-09-08
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: S899- Unspecified injury of lower leg

Interventions

Intervention1: Transdermal Buprenorphine patch: Transdermal Buprenorphine containing 5mg delivering 5mcg/hr

Sponsors

Sri Manakula Vinayagar Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)patients scheduled to undergo orthopaedic surgeries under Spinal anesthesiafrom February 2021 to May 2022. 2)patients of ASA physical status 1 and 2. 3)patients of either sex. 4)Age 18 years to 60 years. 5)patients with height more than 160cm

Exclusion criteria

Exclusion criteria: 1)Body Mass Index >30 2)Patients having chronic pain and on analgesic medications or with prior history of opioid and other substance abuse. 3)patients with local site infection,allergy to the drugs that are tested or any other contraindications for spinal anesthesia. 4)pregnant/Lactating women. 5)patients having failed spinal,transformed into general anesthesia will be excluded from study. 6)patients refusal for participation in the study. 7)patients with height less than 160cm.

Design outcomes

Primary

MeasureTime frame
To assess the effect of preoperative transdermal Buprenorphine patch on subarachnoid block characteristics and compare it with routine spinal anesthesiaTimepoint: 3 hours

Secondary

MeasureTime frame
Time taken for two segment regression,first rescue analgesia between the groups,intraoperative hemodynamic and sedation effectTimepoint: 3 hours

Countries

India

Contacts

Public ContactSuneethPLazarus

Sri Manakula Vinayagar Medical College and Hospital

lazarus.suneeth@gmail.com9894332543

Outcome results

None listed

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