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effect of addition of clonidine to bupivacaine in transversus abdoninis plane block on postoperative pain after lower segment cesarean section

a randomized controlled trial to evaluate the effect of addition of clonidine to bupivacaine in transversus abdoninis plane block on postoperative pain after lower segment cesarean section - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2013/10/004042
Enrollment
100
Registered
2013-10-03
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: null- Healthy Parturients coming for LSCS under spinal anesthesia

Interventions

Intervention1: clonidine 1µgkg-1 added to TAP block with bupivacaine: clonidine 1µgkg-1, bilaterally, added to 20ml of 0.25% bupivacaine, given once as a single injection,in TAP block, following LS

Sponsors

Lady Hardinge Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 100 healthy parturients (ASA physical status I and II) carrying a singleton fetus at term, scheduled to undergo elective LSCS under spinal anaesthesia, followed by a TAP block to relieve postoperative pain

Exclusion criteria

Exclusion criteria: Patients who refused spinal anaesthesia, had any contraindication to regional anaesthesia, had any major co-morbidity or if they were unable to communicate in either English or Hindi language were excluded from this study.

Design outcomes

Primary

MeasureTime frame
The primary outcome will be the duration of postoperative analgesia, defined as the time (in hours) from the giving of the bilateral TAP block with clonidine 1µgkg-1 with 0.25% bupivacaine 20 ml bilaterally or 0.25% bupivacaine 20ml alone to the time to first analgesic request in the postoperative period.Timepoint: time (in hours) from the giving of the bilateral TAP block with clonidine 1µgkg-1 with 0.25% bupivacaine 20 ml bilaterally or 0.25% bupivacaine 20ml alone to the time when patient first demands analgesia in the postoperative period.

Secondary

MeasureTime frame
â?¢the total requirement of analgesics in the first 24hours postoperatively â?¢patients satisfaction and â?¢possible clonidine side effects (nausea and vomiting, sedation, dry mouth , hypotension & bradycardia)Timepoint: . after TAP block, observed every 30 minutes for the first 2 hours, then every hour for next 10 hours and thereafter every 2 hours till the patient demands first dose of analgesia.

Countries

India

Contacts

Public ContactDr Ranju Singh

Lady Hardinge Medical College

slmeena001@gmail.com

Outcome results

None listed

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