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Efficacy of ultrasound-guided erector spinae plane block for analgesia after laparoscopic cholecystectomy: A Randomized controlled trial

Evaluation Of Erector spinae block on quality of postoperative analgesia in Laporoscopic cholecystectomy.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/048691
Enrollment
60
Registered
2023-01-03
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

Health Condition 1: K87- Disorders of gallbladder, biliarytract and pancreas in diseases classified elsewhere Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: erector spinae block: 20 ml of 0.25% bupivacaine given as erector spinae block under ultrasound guidance at beginning of surgery pre intubation and patient will be followed up for 24 hr

Sponsors

Dr challa yaswanth kumar reddy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA I & II AGE: 18-75 yrs

Exclusion criteria

Exclusion criteria: Abnormal coagulation parameters, Patients on antiplatelets, anticoagulants, bleeding, and coagulation disorders. Allergy to study drugs.

Design outcomes

Primary

MeasureTime frame
The primary outcome is to assess the total tramadol doses consumed in the first 24 hrs postoperatively.Timepoint: At the end of 24 hrs—

Secondary

MeasureTime frame
Comparing the duration of effective analgesia Timepoint: Duration is the time from completion of surgery to the point of first post operative pain.;Distribution of VAS SCORETimepoint: 0th,2nd,6th,12th, and 24hrs.—

Countries

India

Contacts

Public Contactchalla yaswanth kumar reddy

sri ramachandra institute of higher education and research

venkymail2014@gmail.com9944731220

Outcome results

None listed

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