comparison between two techniques of labour analgesia
Not Applicable
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated deliveryHealth Condition 2: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2022/10/046613
- Lead Sponsor
- Department of anaesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
patients of 18 to 40 yrs of age with a singleton fetus in cephalic presentation at term with 3 to 5 cm of cervical dilatation who will request labour analgesia with no contraindication
Exclusion Criteria
patient refusal
coagulation disorder
non vertex presentation
raised ict
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method onset of analgesia after interventionTimepoint: 2 to 3 months
- Secondary Outcome Measures
Name Time Method patient satisfaction <br/ ><br>quality of analgesiaTimepoint: 2 to 3 months