MedPath

Comparing effects of Low flow and High flow using Respirometer

Phase 1
Conditions
Health Condition 1: R94- Abnormal results of function studies
Registration Number
CTRI/2019/07/020304
Lead Sponsor
Dr KRISHNA PRASAD T
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

all general anaesthesia cases.

Exclusion Criteria

smoker. lung diseases. ASA 3 and above.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare Vital Capacity between Two GroupsTimepoint: Both Intraoperative and Post operative.
Secondary Outcome Measures
NameTimeMethod
To Compare IRV of both the GroupsTimepoint: 1 hour preoperatively and 1 hour Postoperatively.
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