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A clinical study comparing pain and satisfaction among patients undergoing laparoscopic cholecystectomy surgery

Randomised control trial comparing postoperative pain scores and patient satisfaction in patients undergoing laparoscopic cholecystectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/02/007819
Enrollment
60
Registered
2017-02-08
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- Patients with symptomatic gallstone disease undergoing laparoscopic cholecystectomy surgery

Interventions

Intervention1: Ultrasound guided Combined right Rectus sheath block with right Subcostal Transversus Abdominis Plane block: 40 ml 0.125% bupivacaine with 20 ml in each block injected as a single dose

Sponsors

Self
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Symptomatic gall stone disease patient population undergoing primary laparoscopic cholecystectomy belonging to ASA I-III

Exclusion criteria

Exclusion criteria: Cardio-pulmonary compromise,morbid obesity,conversion to open cholecystectomy/laparotomy,anterior wall hernia defects,combination surgery,past surgery,abdominal trauma,pregnancy

Design outcomes

Primary

MeasureTime frame
Postoperative Pain score measured by visual analog scaleTimepoint: Postoperative pain score measured by visual analog scale 0,2,6,12,24 hours postoperative—

Secondary

MeasureTime frame
Need for rescue analgesia and its DoseTimepoint: 24 hours postoperatively;Patient Satisfaction ScoreTimepoint: 12 and 24 hours postoperative—

Countries

India

Contacts

Public ContactS Ramkiran

AFMC pune

sramkiran44@yahoo.co.in7263957169

Outcome results

None listed

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