Health Condition 1: O- Medical and Surgical Health Condition 2: 1- Obstetrics
Conditions
Interventions
Intervention1: Epidural analgesia: The study population is divided into 2 groups of 27 patients each.
Group A is primigravida females receiving epidural analgesia
Control Intervention1: Normal vaginal
Sponsors
Dr Kalash
Eligibility
Inclusion criteria
Inclusion criteria: 1.The Patient is willing to participate in the study and has provided written informed consent. 2.Term gestation (more than or equal to 37 completed weeks) with a singleton fetus in cephalic presentation 3.Aged 18 years or above (adult women of reproductive age). 4.Classified as ASA physical status II (American Society of Anesthesiologists classification)
Exclusion criteria
Exclusion criteria: 1.Higher ASA status (III or IV), indicating significant systemic disease or complications that pose increased risk. 2.Any high-risk obstetric or medical conditions such as preeclampsia, uncontrolled gestational diabetes, significant cardiac disease, or other comorbidities that could affect labor or anesthesia safety. 3.Contraindications to epidural analgesia or neuraxial blockade, including(local infection,coagulopathy,severe maternal hypotension,neurological disorders,spinal anatomical deformities). 4.Patient refusal.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the alleviation of pain measured by Vas score (visual analog scale)and patient satisfaction score. Timepoint: To compare vas score between two groups at 0 min,30 min,60 min,90 min,120 min and patient satisfaction score at 30 minutes and after 24 hours. | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess maternal & neonatal outcomes. Timepoint: To assess neonatal outcomes by APGAR score at 1 & 5 minutes & maternal outcome by patient satisfaction & mode of delivery. | — |
Countries
India
Contacts
Public ContactDr Ajay Kumar Sinha
Government medical college,Haldwani
Outcome results
None listed