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propofol infusion and antiemetic requirement

Comparison of two different doses of intra operative propofol infusion on post operative rescue antiemetic requiremnt after inhalational anaesthesia - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/094050
Enrollment
50
Registered
2025-09-01
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: PCS- Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: propofol infusion at the rate of 50 microgram per kg per minute: patients recieving propofol infusion at the rate of 50 microgram per kg per minute Control Intervention1: propofol infus

Sponsors

Diana John
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status 1 to 3 BMI 18 to 30

Exclusion criteria

Exclusion criteria: pregnant and lactating patients cardiac, neuro,bariatric surgeries surgical duration more than 6 hours

Design outcomes

Primary

MeasureTime frame
proportion of patients requiring rescue anti emetics in first four hours for PONVTimepoint: proportion of patients requiring rescue anti emetics in first four hours for PONV—

Secondary

MeasureTime frame
number of patients having ponv in first 24 hrs post opTimepoint: first 24 hours;total requirement of rescue antiemetics in 24 hrs post opTimepoint: 24 hrs post op;time to discharge from pacu as per modified aldret score more than nineTimepoint: nil—

Countries

India

Contacts

Public ContactMona Arya

Maulana azad medical college

monaarya@hotmail.com9968604412

Outcome results

None listed

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