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A clinical trial to comparatively evaluate add on effect of dexmedetomidine and propofol for procedural analgosedation with ketamine in short obstetrics and gynecological procedures.

To compare the add on effect of dexmedetomidine and propofol for procedural analgosedation with ketamine in short obstetrics and gynecological procedures. - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/076918
Enrollment
142
Registered
2024-11-18
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: N888- Other specified noninflammatory disorders of cervix uteri

Interventions

Control Intervention1: Ketamine and Dexmedetomidine: Patients will receive a loading dose of 1 mg/kg of ketamine and 1 µg/kg of dexmedetomidine over 3 mins followed by a maintenance infusion of dexmed

Sponsors

Dayanand Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anaesthesiologists (ASA) grade I and II patients. Age group 18-65 years. Short obstetrics and gynaecological procedures(less than 30 minutes)

Exclusion criteria

Exclusion criteria: Patients allergic to the study drugs. Morbidly obese (BMI more than 40 kg/m2 ) Obstructive sleep apnoea. QTc prolongation more than 550 Ms. Second- or third-degree atrioventricular block. Opioid abuser. Patient refusal.

Design outcomes

Primary

MeasureTime frame
comparison of time to first rescue bolus of ketamine between both the groups.Timepoint: Patient assessed every 3 minutes from start to the end of procedure for desired sedation and any procedural interference. Rescue bolus of ketamine will be given if there is any procedural interference or desired sedation is not achieved. Patient will be reevaluated ever 2 minutes

Secondary

MeasureTime frame
Total rescue dose of ketamine, awakening time, recovery time, surgeon satisfaction, recovery agitation, hemodynamic complications and adverse airway effects.Timepoint: Total time of the procedure and the time from the end of the procedure until achieving a modified Aldrete score = 9

Countries

India

Contacts

Public ContactDr Tanveer Singh

Dayanand Medical College and Hospital

singhtanveer09@gmail.com9872828106

Outcome results

None listed

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