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To compare the duration of postoperative analgesia in patients undergoing Laparoscopic cholecystectomy using Magnesium sulphate and Clonidine as adjuvants to Bupivacaine in Transversus Abdominis Plane block.

Comparison of Magnesium sulphate and Clonidine as adjuvant to Bupivacaine in ultrasound guided subcostal Transversus Abdominis Plane block for postoperative analgesia in patients undergoing Laparoscopic cholecystectomy. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072839
Enrollment
60
Registered
2024-08-21
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Ultrasound guided subcostal transversus abdominis plane block: Total 15 ml drug volume consisting of 0.25% bupivacaine + 100 mg magnesium sulphate bilaterally on each side Control Inter

Sponsors

Vardhman Mahavir Medical College and Safdarjung hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged 18-65 years, either gender, belonging to ASA (American Society of Anaesthesiologists) grade I or grade II undergoing laparoscopic cholecystectomy with duration of surgery not exceeding 120 minutes.

Exclusion criteria

Exclusion criteria: 1. Patients allergic to the drugs being used in the study. 2. Infection or inflammation at the site of block application. 3. Patients who have cognitive disability and unable to understand the VAS score.

Design outcomes

Primary

MeasureTime frame
To compare the duration of postoperative analgesia (time to first rescue analgesia as per VAS score) using magnesium sulphate and clonidine as adjuvants to bupivacaine in ultrasound guided transversus abdominis plane block in patients undergoing laparoscopic cholecystectomyTimepoint: postoperatively at 0 hour, 1 hour, 2 hour, 4 hour, 8 hour and 24 hours.

Secondary

MeasureTime frame
1. Total analgesic requirement in 24 hours. 2. To study hemodynamic changes (blood pressure and heart rate) intraoperatively and postoperativelyTimepoint: Intraoperatively and postoperatively

Countries

India

Contacts

Public ContactDr Sujata Chaudhary

Vardhman Mahavir Medical College and Safdarjung hospital

sujatac462@gmail.com9999051546

Outcome results

None listed

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