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

Comparative evaluation of Dexmedetomidine-Ketamine versus Ketamine-Propofol for sedation and analgesia in patients undergoing Dilation and Curettage: A prospective randomized double blind study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050236
Enrollment
80
Registered
2023-03-02
Start date
Unknown
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Health Condition 1: N925- Other specified irregular menstruation

Interventions

Intervention1: inj. Ketamine and Dexmedetomidine: Ketamine 1 mg/kg and Dexmedetomidine 0.5 mcg/kg combined in single syringe given IV slow over 2 min Intervention2: inj propofol and ketamine: inj prop

Sponsors

Ananta institute of medical sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of abnormal uterine bleeding scheduled for elective endometrial sampling American Society of Anaesthesiology I and II

Exclusion criteria

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 •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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
1.Intraoperative Haemodynamics (Heart Rate, Blood Pressure, Spo2, Respiratory rate) 2.Post op recovery score ( Modified Aldrete Score) 3.Duration of analgesia Timepoint: 0min, 10, 20, 30 min

Countries

India

Contacts

Public ContactAnkita Kaasat

Ananta institute of medical sciences

ankitakaasat@gmail.com6361854732

Outcome results

None listed

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