A study to assess the short term and long-term adverse effects oflabour epidural analgesia
Not Applicable
- Conditions
- Health Condition 1: O82- Encounter for cesarean delivery without indicationHealth Condition 2: O80-O82- Encounter for deliveryHealth Condition 3: O618- Other failed induction of laborHealth Condition 4: O00-O9A- Pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2024/04/065143
- Lead Sponsor
- R P PRASHI
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Parturient requesting for labour epidural analgesia
2. Parturient with singleton pregnancy
3. Cephalic presentation with no CPD
Exclusion Criteria
1. Women suffering from back pain before pregnancy due to the diagnosed spinal pathology or past history of back injuries.
2. Epidural contraindications - Coagulopathy, Local site infection, septicemia, Raised ICP
3. Anatomical deformity of Spine
4. Allergy to local anaesthetics
5. Elective C - section
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To find out the outcome of labour in parturients with labour epidural analgesia. (Normal Vaginal Delivery/Instrument assisted delivery/ <br/ ><br>Caeserean Section ) <br/ ><br>Timepoint: 24 hours
- Secondary Outcome Measures
Name Time Method ausea/Vomiting <br/ ><br>Timepoint: 24 hours;PruritisTimepoint: 24 hours;Urinary RetentionTimepoint: 24 hours;Back painTimepoint: 3 months;Duration of 1st and 2nd stage of labourTimepoint: 24 hours;HeadacheTimepoint: 24 hours;HypotensionTimepoint: 24 hours;Motor BlockTimepoint: 24 hours