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Clinical Trials/CTRI/2026/04/107441
CTRI/2026/04/107441Not yet recruitingPhase 4

COMPARING THE EFFECTIVENESS OF KETAMINE-PROPOFOL VERSUS KETAMINE-DEXMEDETOMIDINE COMBINATION IN PATIENTS UNDERGOING HYSTEROSCOPY AND DILATATION AND CURETTAGE PROCEDURES-A RANDOMISED CONTROLLED TRIAL

NORTHERN RAILWAY CENTRAL HOSPITAL1 site in 1 country60 target enrollmentStarted: April 14, 2026Last updated:

Trial Snapshot

Phase
Phase 4
Status
Not yet recruiting
Sponsor
Enrollment
60
Locations
1

Study Overview

Brief Summary

In this study , we aim to determine the best possible combination for opioid-free monitored anaesthesia care using minimal drugs in patients posted for routine hysteroscopy and dilatation and curettage , to shorten recovery time , minimise pain , reduce incidence of post operative nausea vomiting , maintain stable hemodynamics and oxygen saturation while increasing patient’s comfort and surgeon’s convenience

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant and Outcome Assessor Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 65.00 Year(s) (—)
Sex
Female

Inclusion Criteria

  • American Society of Anaesthesiologists Physical status I and II Aged 18-65 years Posted for hysteroscopy or dilatation and curettage procedures Informed consent obtained.

Exclusion Criteria

  • American society of Anaesthesiologists physical status III and above Known allergy to test drugs History of Obstructive sleep apnea Body Mass Index greater than 35 Baseline Oxygen saturation (SPO2) less than 90% Bradycardia (Taken as resting heart rate less than 50 beats per minute to account for individual variations and physiological states) Patient refusal.

Investigators

Sponsor
NORTHERN RAILWAY CENTRAL HOSPITAL
Sponsor Class
Research institution and hospital
Responsible Party
Principal Investigator
Principal Investigator

ABHILASHA TYAGI

NORTHERN RAILWAY CENTRAL HOSPITAL,NEW DELHI

Study Sites (1)

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