A clinical trial to study recommendation based and the effects of local infiltration in patients undergoing laparoscopic cholecystectomy.

A procedure specific Post â?? Operative Pain Management ( PROSPECT) recommendation based prospective randomized observational phase IV study to evaluate local anaesthesia infiltration in patient undergoing laparoscopic cholecystectomy.

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2015/10/006248

Enrollment

Registered

2015-10-12

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- All patients ASA Physical status 1and 2 For laproscopic cholecystectomy.

Interventions

Intervention1: . Intervention- Group A Infilteration of - INJ bupivacaine 0.25%, 5 ml at each trocar site. infilteartion before incision. Compared with group B- INj Bupivaciane Infilteration after in

Eligibility

Inclusion criteria

Inclusion criteria: ASA I â?? II Laparoscopic cholecystectomy using 3-4 ports

Exclusion criteria

Exclusion criteria: Patients refusal Emergency surgery H/o allergic reactionto local anaesthestic drugs Pregnancy and lactating mothers Requiring more than 3 doses of rescue analgesia

Design outcomes

Primary

Measure	Time frame
VAS score for post operative pain Immediate post extubation,Timepoint: 1, 2, 4, 6, 12, 24 hours postoperative	—

Secondary

Measure	Time frame
Number of analgesi demands, pulse, MAP, SpO2Timepoint: 1, 2, 4, 6, 12, 24 hours postoperative	—

Countries

India

Contacts

Public ContactDr Shraddha Mathkar

King Edward Memorial Hospital

m_shrdha@rediffmail.com8879333788

Outcome results

None listed

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