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Effect of lignocaine infusion on postoperative pain relief for patients undergoing abdominal hernia surgery.

Effect of perioperative lignocaine infusion on postoperative pain relief for laparoscopic intraperitoneal onlay mesh repair:a randomised control study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/04/013168
Enrollment
70
Registered
2018-04-11
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- asa physical status Iand II

Interventions

Intervention1: lignocaine: 1.5 mg/kg iv bolus before induction followed by 1.5 mg/kg/hr infusion intraoperatively and 1 hr in PACU. Control Intervention1: placebo: 1.5 mg/kg iv saline(placebo) bolus b

Sponsors

Sir Gangaram hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status I and II, age more than 18 years, scheduled to undergo laparoscopic IPOM surgery

Exclusion criteria

Exclusion criteria: age 70 years

Design outcomes

Primary

MeasureTime frame
POSTOPERATIVE PAIN RELIEFTimepoint: VAS SCORE measured at 2, 4,8,12,24 hours—

Secondary

MeasureTime frame
intraoperative hemodynamic stabilityTimepoint: assessment for 24 hrs;length of hospital stayTimepoint: for 24 hrs;patient satisfactionTimepoint: for 24 hrs;perioperative analgesic consumptionTimepoint: for 24 hrs;postoperative nausea and vomitingTimepoint: for 24 hrs;recovery of bowel functionTimepoint: for 24 hrs—

Countries

India

Contacts

Public ContactDr Rashi Garg

Sir Gangaram Hospital, New Delhi

bimsharma@rediffmail.com8130886280

Outcome results

None listed

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