Comparison of Remifentanil and Fentanyl with AutoFlow mode of ventilation in Laparoscopic surgery

Remifentanil versus Fentanyl along with Autoflow ventilation in Laparoscopic surgery: A Randomized controlled trial - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/10/096512

Enrollment

100

Registered

2025-10-28

Start date

Unknown

Completion date

Unknown

Last updated

2025-11-17

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: inj Remifentanil and inj Fentanyl with AutoFlow ventilation: Remifentanil iv Bolus 1mcg per Kg followed by infusion dose zero point1 mcg per kg per min with AutoFlow ventilation mode

Eligibility

Inclusion criteria

Inclusion criteria: Age 18 to 60 years ASA grade I and II Elective Laparoscopic surgeries and BMI less than 35 Kg per meter square

Exclusion criteria

Exclusion criteria: BMI more than 35 Kg per meter square ASA grade III IV and V Emergency surgeries Pregnancy and Allergies to study drugs

Design outcomes

Primary

Measure	Time frame
To see PIP haemodynamic status time to extubation post operativeTimepoint: At Baseline 15min 30 min 45 min 60 min 90 min 120 min after induction of anaesthesia At extubation	—

Secondary

Measure	Time frame
To assess time of extubation post operative pain score and rescue analgesia requirementTimepoint: Pain score at time of extubation 6 hour after extubation 12 hour and 24 hour after extubation analgesic requirement in 24 hours after surgery	—

Countries

India

Contacts

Public ContactDr Carolin Smita Kerketta

GCS Medical college Hospital and Research Centre Ahmedabad

carolinsmita@gmail.com9904451321

Outcome results

None listed

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