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Effect of Esmolol on pain relief after laparoscopic ventral hernia surgery

Efficacy of intraoperative esmolol infusion on postoperative analgesia in patients undergoing laparoscopic ventral hernia repair : A randomized placebo - controlled trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/063956
Enrollment
34
Registered
2024-03-11
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Intraoperative esmolol infusion: Group E (Esmolol group): Patients in the Esmolol group will receive an IV bolus of esmolol (0.5 mg/kg) i.e 10mg/ml esmolol at a rate of 0.05ml/kg for 10

Sponsors

Sir Gangaram Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 ,2 BMI 18.5-35 Abdominal wall defect size more than 2 cm. in which autofixation device and mesh fixation will be required

Exclusion criteria

Exclusion criteria: Preoperative bradycardia History of chronic opioid use for more than 90 days Patient previously on Beta blocker Patient having received analgesics in preceding 12 hours of surgery HISTORY OF ALLERGY TO MEDICATIONS TO BE USED IN THE STUDY HISTORY OF BRONCHIAL ASTHMA OR AIRWAY HYPER REACTIVITY DECOMPENSATED LIVER,CARDIAC,RENAL OR ENDOCRINE DISEASE REFUSAL TO GIVE CONSENT FOR PARTICIPATION

Design outcomes

Primary

MeasureTime frame
fentanyl citrate consumptionTimepoint: first 24 hours after surgery

Secondary

MeasureTime frame
rescue fentanyl citrate consumption, Pain score, Intraoperative hemodynamic instability, Postoperative sedationTimepoint: at 30 minutes, 1 hour, 2 hours, 6 hours, 12 hours and 24 hours post-operatively.

Countries

India

Contacts

Public ContactDr. Anil Kumar Jain

Sir Gangaram Hospital,New Delhi

ms28081984@gmail.com9896044430

Outcome results

None listed

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