MedPath

A clinical study to find after effects related to performance conditions in patients after treatment of cardiac arrest who are already admitted in neurosurgery ICU.

Not Applicable
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2024/07/070921
Lead Sponsor
All India Institute of medical sciences New Delhi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Written informed consent from relative / attendant

2.All neurosurgical and neurological critically ill patients who achieve reversal of spontaneous circulation [ROSC]after in-hospital cardiac arrest

Exclusion Criteria

Patient does not achieve ROSC after cardiac arrest

Out of hospital cardiac arrest with ROSC

AGE less than 18 years

Non consenting relative or attendant

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Neurological outcome assessed using Glasgow outcome scale extended at 3 and 6 months <br/ ><br>2. Factors (demographic and disease related) affecting the outcome of patients at 3 and 6 months.Timepoint: 1. at 3 and 6 months <br/ ><br>2. Factors assessment at 1st hr, 24hr, and 5th day post ROSC <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
Consciousness assessment at 1 hour, 24 hour and 5th day post ROSC ( assessed using GCS-P)Timepoint: At 1 hour, 24 hour, 5th day post ROSC;Hospital length of stayTimepoint: Duration of hospital admission;ICU length of stayTimepoint: Duration of ICU stay;MortalityTimepoint: Till 6th month post ROSC;Post cardiac arrest complicationsTimepoint: At hospital stay period, 3 months and 6 months post ROSC
© Copyright 2025. All Rights Reserved by MedPath