MedPath

Comparison of post operative pain relief in cesarean delivery with buprenorphine and morphine when used along with 0.25%bupivacaine in ultrasound guided transversus abdominis plane block.

Phase 2/3
Not yet recruiting
Conditions
Medical and Surgical,
Registration Number
CTRI/2021/07/035203
Lead Sponsor
M MUGUNDA RAJ
Brief Summary

Post operative pain in cesarean delivery is of utmost concern, inadequate pain relief may lead to Poor recovery and prolong hospital stay. Hence it require a multimodal approach, as transversus abdominis plane has extended course of subcostal, ilioinguinal, iliohypogatric and genitofemoral nerves.A transversus abdominis plane (TAP) block is more appropriate in lower abdominal surgeries.As blind injections can result in inadvertent injury to bowel or blood vessels using ultrasound guided transversus abdominis plane block is more is more appropriate. Bupivacaine has shown its efficacy in providing post operative analgesia for 6 to 8hours adding an adjuvant will prolong its effect.In this study we are about to compare the post operative analgesic effect of buprenorphine and morphine when added as adjuvant to 0.25% bupivacaine in ultrasound guided transversus abdominis plane block, in patient undergoing cesarean delivery.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
Female
Target Recruitment
70
Inclusion Criteria

Patient with ASA physical status-2 posted for cesarean delivery.

Exclusion Criteria
  • Chronic pain disorder 2.
  • Known allergy or hypersensitivity to the study drug 3.
  • Coagulopathy 4.local infection at block site 5.patient refusal for the procedure.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Heart rate,All these parameters are measured every 15mins for 1st hour,then every hourly upto 12hours,Then every 4th hourly upto 24hours.
Post operative pain assessment (VAS score),All these parameters are measured every 15mins for 1st hour,then every hourly upto 12hours,Then every 4th hourly upto 24hours.
Respiratory rate,All these parameters are measured every 15mins for 1st hour,then every hourly upto 12hours,Then every 4th hourly upto 24hours.
Blood pressure,All these parameters are measured every 15mins for 1st hour,then every hourly upto 12hours,Then every 4th hourly upto 24hours.
Oxygen saturation.All these parameters are measured every 15mins for 1st hour,then every hourly upto 12hours,Then every 4th hourly upto 24hours.
Secondary Outcome Measures
NameTimeMethod
24 hour analgesic consumption, nausea, vomiting, pruritis,Monitored for 24 hours

Trial Locations

Locations (1)

Sri manakula vinayagar medical college and hospital

🇮🇳

Pondicherry, PONDICHERRY, India

Sri manakula vinayagar medical college and hospital
🇮🇳Pondicherry, PONDICHERRY, India
M MUGUNDA RAJ
Principal investigator
9894228804
mugunthraj94@gmail.com

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.