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COMPARISION OF TWO DRUG GROUPS FOR SEDATION IN ADULTS UNDERGOING SHORT SURGICAL PROCEDURES

INTRAVENOUS DEXMEDETOMIDINE-KETAMINE VERSUS KETAMINE-PROPOFOL FOR PROCEDURAL SEDATION IN ADULTS UNDERGOING SHORT SURGICAL PROCEDURES: A RANDOMISED CONTROLLED TRIAL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/09/036768
Enrollment
194
Registered
2021-09-23
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: N979- Female infertility, unspecified Health Condition 2: N719- Inflammatory disease of uterus, unspecified Health Condition 3: O- Medical and Surgical

Interventions

Intervention1: PROCEDURAL SEDATION: TWO DIFFERENT DRUG COMBINATIONS WILL BE GIVEN FOR SEDATION IN ADULTS UNDERGOING SHORT SURGICAL PROCEDURES. Group KD- The subjects will receive: For induction -

Sponsors

ANUSHA KAKARLA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status grade I / II posted for elective procedures of duration less than thirty minutes

Exclusion criteria

Exclusion criteria: Patients who are allergic to the drugs used in study, Pregnant women, Patients with Obstructive Sleep Apnea

Design outcomes

Primary

MeasureTime frame
TO COMPARE EFFICACY BETWEEN TWO DRUGS BASED ON TOTAL NUMBER OF RESCUE BOLUS DOSES OF KETAMINE NEEDED DURING PROCEDURE.Timepoint: During the surgical procedure—

Secondary

MeasureTime frame
TO COMPARE EFFICACY BETWEEN TWO DRUGS BASED ON FOLLOWING PARAMETERS: procedural interference, time taken for first rescue bolus, hemodynamics and pain score. To compare surgeon satisfaction , patient satisfaction between two groups.Timepoint: every 3 minutes till the end of the procedure.—

Countries

India

Contacts

Public ContactDR AMIT PRADHAN

KALINGA INSTITUTE OF MEDICAL SCIENCES

amit.pradhan@kims.ac.in9437191002

Outcome results

None listed

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