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To evaluate bilateral versus unilateral erector spinae plane block for postoperative analgesia in patients undergoing laparoscopic cholecystectomy

To evaluate bilateral versus unilateral erector spine plane block for postoperative analgesia in patients undergoing laparoscopic cholecystectomy - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/063085
Enrollment
72
Registered
2024-02-23
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: K80- Cholelithiasis

Interventions

Intervention1: Unilateral Erector spinae plane block: Under all aseptic precautions, the probe will be placed longitudinally 3cm lateral to the T8 level.Following identification of the transverse proc

Sponsors

Pt B D Sharma PGIMS Rohtak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients of either gender, aged 18-60 years belonging to American society of Anaesthesiologists (ASA) I-II scheduled for elective laparoscopic cholecystectomy under general anaesthesia will be included in the study.

Exclusion criteria

Exclusion criteria: Patients with : Contraindications to regional anaesthesia such as coagulopathy, infection at the site of puncture etc. Known history of hypersensitivity/anaphylaxis/contraindications to bupivacaine or its components Pregnancy Mental disorders/o Illness BMI >35kg/m2 Chronic drug/analgesic abuse Refusal to give consent Severe renal or liver diseases Will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
To compare post operative numerical rating scale (NRS) for pain following bilateral versus right sided ESPB in patients undergoing laparoscopic cholecystectomy.Timepoint: Score at rest and score on coughing at 15 min 1 hr 6 hr 24 hr

Secondary

MeasureTime frame
Block related complications, if anyTimepoint: Block related complications, if any;Duration of postoperative analgesiaTimepoint: Duration of postoperative analgesia (in hours);Postoperative nausea and vomitingTimepoint: Postoperative nausea and vomiting;Total analgesic consumption in 24hrsTimepoint: Total analgesic consumption in 24hrs

Countries

India

Contacts

Public ContactDr Urmi Malik

Pt B D Sharma PGIMS Rohtak

Kamalkirti47@gmail.com9215650615

Outcome results

None listed

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