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Compare recovery profile of propofol administered by manual infusion with target controlled infusion in gynaecological surgeries

Comparison of Target Controlled Infusion with Manual Infusion of Propofol on Post-operative recovery in patients undergoing Gynaecological Endoscopic Procedures – An Open-label Randomized controlled trial.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050936
Enrollment
100
Registered
2023-03-21
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: N839- Noninflammatory disorder of ovary,fallopian tube and broad ligament, unspecified

Interventions

Intervention1: Target controlled infusion of propofol: Continuous infusion of Propofol by TCI pump set to plasma level of 4mcg/ml till end of surgery Control Intervention1: Manual infusion of propofol

Sponsors

SRM Medical College Hospital and research centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients posted for Gynaecological Endoscopic surgeries 2. Age 18 year to 65 year 3. ASA I/II

Exclusion criteria

Exclusion criteria: 1. Non-consenting patients 2. Uncontrolled co-morbid illness 3. Hypersensitivity/allergy to propofol 4. Patients with psychiatric disorders 5. Patients with opioid dependency

Design outcomes

Primary

MeasureTime frame
To compare the time taken to recover as assessed by time taken to obey simple commands after termination of propofol infusion in both techniquesTimepoint: After end of surgery—

Secondary

MeasureTime frame
1. Total dose of propofol administered (mg/kg/hr) 2. Change in Mean Arterial Pressure (MAP) post-inductionTimepoint: End of surgery—

Countries

India

Contacts

Public ContactKavin NS

SRM Medical College hospital and research centre

anandk@srmist.edu.in9865282288

Outcome results

None listed

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