None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion criteria Patient of age group of 18-30 years, planning to give birth electively via normal vaginal route American Society of Anesthesiologists (ASA)physical status I-III Singleton pregnancy
Exclusion criteria
Exclusion criteria: Exclusion criteria Patient refusal Infection at intervention site Coagulation disorder Intracranial pathology Allergy to study drugs Active neurological/Psychiatry disease Complicated obsteteic conditions [ twin,GDM,SPE]
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To determine the efficacy of epidural labor analgesia in prevention of postpartum depression using Edinburgh Postnatal Depression Scale [EDPS] Timepoint: At 2weeks 4weeks 6weeks from date of delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| To study the effect of epidural analgesia on duration of labour To study the effect of epidural analgesia on fetal outcome using APGAR score To study the maternal satisfaction using Maternal satisfaction scale.Timepoint: Pain [ vas score] measure before epidural, 30min after epidural, 2Hourly upto delivery of the baby APGAR score measure at 1min & 5min maternal satisfaction score after 24hrs of epidural catheter placement | — |
Countries
India
Contacts
Kgmu Lucknow up