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Study is based on comparison on induction time and dose requirement of propofol with nitrous oxide used during induction

effect of inhaled nitrous oxide on induction time and dose requirement of propofol a prospective randomised study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/03/041441
Enrollment
60
Registered
2022-03-29
Start date
Unknown
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

Health Condition 1: R69- Illness, unspecified Health Condition 2: O- Medical and Surgical

Interventions

Control Intervention1: COMPARATOR: PATIENT WILL BE GIVEN NITROUS OXIDE DURING INDUCTION ALONG WITH OXYGEN TO COMPARE THE DOSE REQUIREMENT FOR PROPOFOL AND INDUCTION TIME FOR PATIENT

Sponsors

Dr Mankeerat Kaur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American society of anaesthesiologists (ASA) 1 and 2 age range 18-60 any elective minor or major surgery requiring general anaesthesia

Exclusion criteria

Exclusion criteria: pregnancy morbid obesity bronchial asthma diabetes mellitus drug allergy relative contraindications ( intestinal obstruction, middle ear disease, pneumothorax, air embolism)

Design outcomes

Primary

MeasureTime frame
to study the effects of inhaled N2O in reducing the induction dose requirements of propofol with induction timeTimepoint: 8 WEEKS—

Secondary

MeasureTime frame
to study the haemodynamic variations and adverse effects of inhaled N2OTimepoint: time (minutes) - 0, 2, 4, 6, 10—

Countries

India

Contacts

Public ContactDr Mankeerat Kaur

D.Y.Patil Medical School

varsha.vyas011@gmail.com9819583232

Outcome results

None listed

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