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comparison of two drugs for anaesthesia during dilation and curettage in females with abnormal menstrual bleeding

Not Applicable
Conditions
Health Condition 1: N925- Other specified irregular menstruation
Registration Number
CTRI/2023/03/050236
Lead Sponsor
Ananta institute of medical sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients of abnormal uterine bleeding scheduled for elective endometrial sampling

American Society of Anaesthesiology I and II

Exclusion Criteria

History of cardiovascular diseases e.g. ischemic heart disease, conduction defects, etc.

History of compromised renal / hepatic / neuronal functions.

Uncontrolled Hypertension and Diabetes

History of alcohol, substance abuse, chronic use of analgesic and sedatives, psychiatric disorders

•Patients on beta blocker or having persistent bradycardia with HR <60.

•Drug allergy

•Procedure lasting for >30 min.

•Any surgical complications during D& C e.g. uterine perforation, excessive bleeding etc.

•Viable Pregnancy, acute PID, undiagnosed genital tract bleeding, mass in vagina or cervix, severe arthritis hip bone, bleeding disorders, virgin females

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time to onset of sedation (Ramsay sedation score RSS 6) and recovery from sedation (RSS 3)Timepoint: Time to onset of sedation (Ramsay sedation score RSS 6) and recovery from sedation (RSS 3)
Secondary Outcome Measures
NameTimeMethod
1.Intraoperative Haemodynamics (Heart Rate, Blood Pressure, Spo2, Respiratory rate) <br/ ><br>2.Post op recovery score ( Modified Aldrete Score) <br/ ><br>3.Duration of analgesia <br/ ><br>Timepoint: 0min, 10, 20, 30 min
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