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To see the effect of external oblique intercostal plane block on post operative pain relief in patients for laparoscopic cholecystectomy.

Efficacy of bilateral external oblique intercostal plane block for postoperative pain relief in patients undergoing laparoscopic cholecystectomy. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071108
Enrollment
44
Registered
2024-07-23
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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 bilateral external oblique intercostal plane block (EOIPB): USG guided EOIPB will be administered at the end of surgery.It will take around 10-15 mins. Control Interve

Sponsors

Pt BD Sharma PGIMS Rohtak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American society of Anesthesiologists (ASA) physical status I to II, scheduled to undergo Laparoscopic cholecystectomy (LC) under general anaesthesia will be included in the study.

Exclusion criteria

Exclusion criteria: Patients with allergy to local anaesthetics, coagulopathies, pregnancy, infection at local site, weight less than 45kg and BMI more than 35 kg/m², chronic opioid use, history of abdominal surgery, refusal to consent.

Design outcomes

Primary

MeasureTime frame
To evaluate analgesic consumption (tramadol and paracetamol) in the first 24 hours in both groups.Timepoint: To evaluate analgesic consumption(tramadol and paracetamol) at 30 mins, 1hr, 2hr,6hr, 12hr and 24hrs post operatively in both groups.

Secondary

MeasureTime frame
1.Postoperative pain score evaluation using visual analogue scale (VAS) in PACU at 30 min, 1 h, 2h, 6h. 12h and 24h postoperatively 2.Time of first analgesic request. 3.Postoperative Nausea and Vomiting (PONV) 4.Sedation score 5.Number of dermatomes anaesthetised. 6.Adverse effects (if any) Timepoint: At 30 min, 1h, 2h, 6h. 12h and 24h postoperatively.

Countries

India

Contacts

Public ContactDr Aishwara Tamboli

Department of Anaesthesiology , Pandit BD Sharma PGIMS Rohtak.

drbmamta@gmail.com9812789476

Outcome results

None listed

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