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To compare the efficacy of only Ketamine and Ketamine - Dexmedetomidine in reducing propofol dose for IV sedation in short gynaecological procedures

Efficacy of Ketamine versus Ketamine ? Dexmedetomidine on effect site concentration of propofol target controlled infusion in short gynaecological procedures ? Randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093580
Enrollment
90
Registered
2025-08-25
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Ketamine- Propofol: Patients receiving Ketamine at dose of 0.75 mg/kg bolus with Propofol TCI at baseline effect site concentration of 2.0 mcg/ml. The patient will be assessed every 3 m

Sponsors

Sri Manakula Vinayagar Medical College Hospital Kalitheerthalkuppam Madagadipet
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age 18 ? 60 years Female Gender Patients posted for elective short gynaecological procedures ASA Physical Status I to III

Exclusion criteria

Exclusion criteria: Refusal to give informed consent

Design outcomes

Primary

MeasureTime frame
To compare the Effect site concentration of propofol TCI with only ketamine and with ketamine dexmedetomidineTimepoint: Baseline, 3 minutes, 6 minutes, 9 minutes, 12 minutes, 15 minutes, 18 minutes, 21 minutes, 24 minutes, 27 minutes, 30 minutes

Secondary

MeasureTime frame
To assess the incidence of intraoperative airway events in both group To assess the hemodynamics during the procedure in both groups To assess the recovery time in both groupsTimepoint: 0-30 minutes

Countries

India

Contacts

Public ContactNithiyasree S

Sri Manakula Vinayagar Medical College Kalitheerthalkuppam Madagadipet Puducherry

ranjanrv2005@gmail.com9600823772

Outcome results

None listed

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