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A clinical trial to study effect of bupivacaine for post operative pain in patients undergoing surgery for gall stone disease laparoscopically

Efficacy of high-volume low- concentration intraperitoneal bupivacaine irrigation for post operative analgesia in patients undergoing laparoscopic cholecystectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/02/017802
Enrollment
30
Registered
2019-02-25
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

None listed

Interventions

Intervention1: bupivacaine(study) group: 20 ml of 0.5% bupivacaine(100mg) added to 480 ml of normal saline which will then be used for intraperitoneal irrigation Control Intervention1: normal saline g

Sponsors

SWATI PANWAR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA PHYSICAL STATUS I/II 2. SCHEDULED FOR ELECTIVE LAPAROSCOPIC CHOLECYSTECTOMY UNDER GENERAL ANAESTHESIA

Exclusion criteria

Exclusion criteria: 1. ALLERGY TO LOCAL ANAESTHETICS 2. ACUTE PANCREATITIS 3. CHOLEDOCHOLITHIASIS 4. CURRENT ANALGESIC USE 5. INABILITY TO COMPREHEND NRS( NUMERIC PAIN RATING SCALE) 6. PREGNANCY

Design outcomes

Primary

MeasureTime frame
DURATION OF ANALGESIATimepoint: time interval between removal of airway device and first requirement of rescue analgesic—

Secondary

MeasureTime frame
-NUMERIC PAIN RATING SCALE -TOTAL DOSE OF RESCUE ANALGESIC IN 24 HRS -INCIDENCE OF SHOULDER PAIN -INCIDENCE OF NAUSEA AND VOMITINGTimepoint: IMMEDIATELY AFTER EXTUBATION 15 MIN. 30 MIN. 1,2,4,6,8,12,24 HRS—

Countries

India

Contacts

Public ContactDR SWATI PANWAR

MAULANA AZAD MEDICAL COLLEGE

dr_dali@rediff.com9968604212

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 6, 2026