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Comparison of sleep-induction time between standard and diluted Propofol for patients undergoing tubal ligation surgery.

Comparing Induction Time Of Standard Vs Diluted Concentration Of Propofol In Patients Undergoing Laproscopic Tubal Ligation A Randomized Controlled Study - NIL

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104713
Enrollment
76
Registered
2026-02-25
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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: 0.5% Propofol: 1 ml 1% Propofol diluted with 1ml 5% Dextrose final concentration: 5 mg/mL patients will received 0.5% propofol Intravenously in a syringe pump at 99ml/hour until loss of

Sponsors

DrBabasaheb ambedkar medical college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Female patients aged 18-45 years. 2.Scheduled for laparoscopic tubal ligation under general anaesthesia. 3.ASA physical status I or II. 4.Body Mass Index (BMI) 18 30 kg/m .

Exclusion criteria

Exclusion criteria: 1.Known allergy to propofol, egg, or soy products. 2.Cardiovascular disease: uncontrolled hypertension, arrhythmias, ischemic heart disease. 3.Respiratory disease: severe asthma, COPD. 4.Hepatic or renal dysfunction. 5.History of difficult airway or anticipated airway problems. 6.Patients on medications that interfere with anesthetic drugs (e.g., chronic sedatives, anticonvulsants). 7.Any neurological or psychiatric disorder affecting assessment of consciousness

Design outcomes

Primary

MeasureTime frame
Time of beginning of infusion to time to loss of verbal response will be induction time(min)Timepoint: 3 months

Secondary

MeasureTime frame
Hemodynamic changes like systolic & diastolic blood pressure, heart rate, respiratory rate, pulse oximetry, endtidal- carbon dioxide will be recorded before induction, at the end of induction & 5 minutes after induction. Any Episodes of apnea will be noted,apnea is defined as observation of a cessation of breathing (10 or more seconds) by the patient,which is confirmed using capnography Total dose of propofol required for induction recorded (mg/kg) Injection pain will be assessed at the start of propofol administration using a Visual Analog Scale (VAS 0 10).Timepoint: 3 months

Countries

India

Contacts

Public ContactDr Neetu Chaudhary

Dr.Baba Saheb Ambedkar Medical Collage And Hospital,Rohini,New Delhi

dr.neetu.hrc@gmail.com7065023138

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026