A study of dexmedetomidine-ketamine versus propofol-ketamine sedation in females undergoing dilatation and evacuation in obstetrics and gynaecology patients

A COMPARATIVE STUDY OF DEXAMEDETOMINDINE- DETAMINE VERSUS PROPOFOL-DETAMINE FOR PROCEDURAL SEDATION IN FEMALES UNDERGOING DILATATION AND EVACUATION IN OBSTETRICS AND GYNAECOLOGY PATIENTS - nil

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/03/063830

Enrollment

117

Registered

2024-03-08

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-01

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

Conditions

Health Condition 1: 1- Obstetrics

Interventions

Intervention1: comparison of dexmedetomidineketamine with ketamine propofol in dilatation and evacuation procedure in obstetrics and gynaecology patient: comparison of haemodynamics and postoperative

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 and ASA 2

Exclusion criteria

Exclusion criteria: allergy to given drug , electrolyte disorder , severe liver disese , kidney disease ,severe heart diseases , refusal to given drug ,

Design outcomes

Primary

Measure	Time frame
To compare the hemodynamic response of drug combination ketamine propofol -dexmedetomidine ketamine in dilatation and evacuation proceduresTimepoint: 18 months	—

Secondary

Measure	Time frame
to compare postoperative pain using visual analogue score postoperative delirium postoperative sedation surgeon satisfactionTimepoint: 18 months	—

Countries

India

Contacts

Public ContactDr Ajay Kumar Sinha

Government Medical College and Dr STM Hospital, Haldwani, Uttarakhand

sinhaak1961@gmail.com9897672301

Outcome results

None listed

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