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Comparative evaluation of the effect of Clonidine and Atenolol premedication on hemodynamic effects and Propofol dose requirement in patients undergoing ERCP under monitored anesthesia care: a double blind, randomized, placebo controlled study.

Comparative evaluation of the effect of Clonidine and Atenolol premedication on hemodynamic effects and Propofol dose requirement in patients undergoing ERCP under monitored anesthesia care: a double blind, randomized, placebo controlled study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2012/05/002643
Enrollment
114
Registered
2012-05-10
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- Patients undergoing ERCP under monitored anaesthesia care at SGPGI, Lucknow

Interventions

Intervention1: Clonidine (4 mck/kg): Route of administration: Oral Dose 4 mcg/kg single dose Half life 12 hours Control Intervention1: Atenolol 25mg: Route of administration: oral Dose 25mg single do

Sponsors

SGPGI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: > 18yrs, Undergoing elective ERCP (diagnostic or therapeutic) under monitored anaesthesia care

Exclusion criteria

Exclusion criteria: Consent not given Patients already on Atenolol or Clonidine or on Cardiac Drugs. Heart rate less 60 per min or Blood Pressure less than 100mgHG systolic. Pregnant patients. Emergency procedure. ASA more than or equal to 4 patients Patients requiring airway intervention or general anaesthesia. Expected duration less than 30min or more than 2hours. Patients with history of drug abuse or allergy to the drugs to be used.

Design outcomes

Primary

MeasureTime frame
To evaluate the effectiveness of Atenolol and Clonidine premedication in preventing hemodynamic stress and myocardial injury in patients undergoing ERCP under sedation.Timepoint: During procedure and 24 hours after procedure.

Secondary

MeasureTime frame
1.To study the occurrence of adverse effects during ERCP. 2.To study the hemodynamic response to Buscopan administration. 3.To study the dose requirement of Propofol during the procedure and the effect of Atenolol and Clonidine premedication on it. 4.To assess the patient and operator satisfaction with procedures under sedation in our institution. 5.To evaluate the time of awakening and discharge to ward. Timepoint: during procedure and 24 hours after the procedure

Countries

India

Contacts

Public ContactDr Devendra Gupta

SGPGI, Lucknow

dgupta@sgpgi.ac.in8004904595

Outcome results

None listed

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