Comparative evaluation of two drug combinations of propofol-ketamine and propofol-fentanyl for total intravenous anaesthesia in short surgical procedures

Comparative evaluation of propofol-ketamine and propofol-fentanyl for short surgical procedures

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/06/019790

Enrollment

120

Registered

2019-06-20

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: O- Medical and Surgical

Interventions

Intervention1: Propofol-ketamine: Comparison in terms of intra operative hemodynamics, post operative nausea vomiting, depth of sedation, time for recovery and time to rescue analgesics. Control Inter

Eligibility

Inclusion criteria

Inclusion criteria: Patients belonging to ASA 1 and 2 posted for elective surgical procedures lasting for less than 60 minutes, not requiring a difficult airway.

Exclusion criteria

Exclusion criteria: Patients belonging to ASA 3 4 History of allergy to any particular drug used in the study History of egg allergy History of opioid or substance abuse

Design outcomes

Primary

Measure	Time frame
To compare the hemodynamic and respiratory parameters in the intra operative period.Timepoint: To compare the hemodynamic and respiratory parameters in the intra operative period.	—

Secondary

Measure	Time frame
To study the incidence of post operative nausea vomiting, depth of sedation, time to discharge from the PACU, and total dose of study drugs usedTimepoint: Every 15 min from shifting the patient to PACU , till discharge from PACU	—

Countries

India

Contacts

Public ContactDr Amrita Panda

Kalinga institute of medical sciences

amritapanda1323@gmail.com9439862335

Outcome results

None listed

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