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To evaluate the effect of local anaesthetic with or without dexmedetomidine for post operative pain relief in laparoscopic gall bladder surgery

Comparative evaluation of ropivaciane with or without dexmedetomidine in ultrasound guided transversus abdominis plane (TAP) block for postoperative analgesia after laparoscopic cholecystectectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2013/07/003841
Enrollment
100
Registered
2013-07-25
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

Health Condition 1: null- Cholelithiasis

Interventions

Intervention1: To evaluate the relative efficacy of ropivacaine(0.375%) in USG TAP block for post opeartive pain relief in patients scheduled for laparoscopic cholecystectomy: To evaluate the relative

Sponsors

Director principal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • ASA physical status I-II • Age 18-65 yrs • Body weight 50-75 kg of either sex BODY MASS INDEX ( > 18 -

Exclusion criteria

Exclusion criteria: • History of relevant drug allergy • Age 65yrs • History of psychiatric illness , substance abuse ,or medical therapies resulting in tolerance to opioids • Acute cholecystitis or pancreatitis • Severe cardiovascular , respiratory , metabolic, or neurological disease • Surgery requiring postoperative intraabdominal drainage • Pregnancy

Design outcomes

Primary

MeasureTime frame
To evaluate the relative efficacy of ropivacaine with or without dexmedetomidine in ultrasound guided transversus abdominis plane (TAP) block for postoperative analgesia after laparoscopic cholecystectomyTimepoint: 10 min, 30 min, 1 hr, 4hr, 8hr, 12 hr and 24 hrs in the post operative period—

Secondary

MeasureTime frame
To calculate the total dose of rescue analgesic over 24 hours in both the groups, and to evaluate postoperative nausea and vomiting and to calculate the dose of antiemetic over 24 hours. To note any side effects pertaining to the drugs being used Timepoint: Over 24 hrs—

Countries

India

Contacts

Public ContactDR RICHA SAROA

GOVERNMENT MEDICAL COLLEGE AND HOSPITAL SECTOR-32/B

sanjeev_palta@yahoo.com9646121523

Outcome results

None listed

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