Skip to content

A comparison study of different methods to check for fitness before major non-cardiac surgery.

A prospective observational comparative study: assessing functional capacity to predict 90-day mortality and/or morbidity after major non-cardiac surgery in a cohort of hilly population of Uttarakhand

Status
Recruiting
Phases
Phase 3Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/03/012779
Enrollment
500
Registered
2018-03-23
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: null- patients undergoing major noncardiac surgery Health Condition 2: I279- Pulmonary heart disease, unspecified

Interventions

None listed

Sponsors

All India Institute of Medical Sciences Rishikesh
Lead Sponsor
All India Institute of Medical Sciences Rishikesh
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: All Patient must be 18 years or old of either sex and scheduled to undergo elective noncardiac surgery (with exception of cataract and plastic surgeries) under general or regional anaesthesia with scheduled stay in hospital for at least one day

Exclusion criteria

Exclusion criteria: pregnancy, active cardiac conditions, emergency surgeries, low risk surgeries (superficial surgery under Local anesthesia, cataract surgery and plastic surgery) and absolute contraindication to 6MWT. Absolute contraindication to 6MWT are Unstable angina or myocardial infarction during the previous month and relative contraindication include a resting heart rate of > 120/min and systolic blood pressure > 180 mm Hg and diastolic blood pressure of more than 100 mm Hg.

Design outcomes

Primary

MeasureTime frame
To compare CPET with other methods of functional assessment to predict all cause death or nonfatal morbidity within 90 days after surgery.Timepoint: 3 year

Secondary

MeasureTime frame
To assess the possibility of replacing CPET with other methods. To assess sensitivity and specificity of each method. To study cost effective ness of each method. Timepoint: 90 days

Countries

India

Contacts

Public ContactNishith Govil

All India Institute of Medical Sciences, Rishikesh

nishithgovil@rediffmail.com8126101759

Outcome results

None listed

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