A clinical trial to check for association of preoperative hand grip strength with perioperative hemodynamic changes in patients undergoing cesarean section under subarachnoid block
Not Applicable
- Conditions
- Health Condition 1: O94-O9A- Other obstetric conditions, not elsewhere classified
- Registration Number
- CTRI/2024/01/061946
- Lead Sponsor
- Dayanand Medical College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA 2 and ASA 3 pregnant females aged 18 and above
Exclusion Criteria
1. Parturients who cannot use the dynamometer
freely or are unable to comprehend the commands.
2. Parturients with movement restriction in upper limbs or having positive history of any neurological disorder.
3. Parturients who are hemodynamically unstable or in severe cardiopulmonary distress.
4. Parturients with history of allergy to local anaesthetics.
5. Parturients with cord prolapse, ruptured uterus, eclampsia, altered sensorium, fetal distress, morbidly adherent placenta or placenta
accreta.
6. Parturients with any contraindication to subarachnoid block.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method