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To evaluate the effectiveness of oral clonidine as a premedication on intraoperative hemodynamic response for patients undergoing laproscopic cholecystectomy- A Single Blinded Randomised Control Study

Effectiveness of oral clonidine as a premedication on intraoperative hemodynamic response for patients undergoing laproscopic cholecystectomy- A Single Blinded Randomised Control Study - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079642
Enrollment
102
Registered
2025-01-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: K80- Cholelithiasis

Interventions

Intervention1: Hemodynamic response and postoperative analgesic requirement: Premedication with oral clonidine 100mcgs versus vitamin C 1 hour before surgery to assess intraoperative hemodynamic respo

Sponsors

SRI RAMACHANDRA MEDICAL COLLEGE AND RESEARCH HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grading 1 and 2 Elective laproscopic surgery under general anaesthesia. BMI less than 30kg/m2

Exclusion criteria

Exclusion criteria: Patient refusal for consent. ASA grading more than 3. BMI more than 30kg/m2

Design outcomes

Primary

MeasureTime frame
Intraoperative hemodynamic response( HR, BP, MAP, sevoflurane concentration, total vasopressors used, total amount of fluids given)Timepoint: Baseline, 1 min after intubation, 5mins after intubation, time of skin incision, at time of pneumoperitoneum, 15 mind after pneumoperitoneum, 15mins after release of pneumoperitoneum.

Secondary

MeasureTime frame
Postoperative analgesic requirement VAS SCORES RAMSAY SEDATION SCORETimepoint: 30 mins, 60 mins, 90 mins, 120 mins postoperative period

Countries

India

Contacts

Public ContactKARTIK RAJGOPAL L

Sri Ramachandra medical college and research hospital

vjram2001@yahoo.co.in9841219820

Outcome results

None listed

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