Health Condition 1: O82- Encounter for cesarean delivery without indication Health Condition 2: O80-O82- Encounter for delivery Health Condition 3: O618- Other failed induction of labor Health Condition 4: O00-O9A- Pregnancy, childbirth and the puerperium
Conditions
Interventions
Control Intervention1: NIL Intervention: Control group will be chosen by the Obstetrician with similar demographics
similar to Epidural group. The control group will be given other modes of Analgesia.
Sponsors
L R P PRASHIN
Eligibility
Inclusion criteria
Inclusion criteria: 1. Parturient requesting for labour epidural analgesia 2. Parturient with singleton pregnancy 3. Cephalic presentation with no CPD
Exclusion criteria
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To find out the outcome of labour in parturients with labour epidural analgesia. (Normal Vaginal Delivery/Instrument assisted delivery/ Caeserean Section ) Timepoint: 24 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| Nausea/Vomiting 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 | — |
Countries
India
Contacts
Public ContactANITA SHIRLEY JOSELYN
Christian Medical College
Outcome results
None listed