Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Parturients in established labour with cervical dilation 3-5 c.m. and having satisfactory uterine contractions. 2) Singleton pregnancy with vertex presentation at term. 3) Primigravida or gravida 2. 4) Age 18 years or above, weight less than 100kg, height 150 cm or more.
Exclusion criteria
Exclusion criteria: 1) Patient refusal. 2) Any fetal anomalies. 3) History of coagulation disorders. 4) Any contraindications to neuraxial anaesthesia. 5) History of allergy to local anaesthetics. 6) Any obstetric complications. 7) Medical disorders complicating pregnancy (i.e., preeclampsia, gestational diabetes). 8) Increased risk of a cesarean delivery (i.e., history of uterine anomaly or surgery, morbid obesity,Previous LSCS).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1)To evaluate total consumption of local anaesthetic& fentanyl for duration of epidural labour analgesia. 2)Presence of sacral dermatome (S1) blockade (either unilateral or bilateral). 3)To observe the effect of ropivacaine and fentanyl on duration of labour and side effects, if any. 4)To evaluate the maternal satisfaction. 5)To assess the incidence of breakthrough pain. Timepoint: Till Delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)To evaluate the effect of ropivacaine and fentanyl on maternal haemodynamic parameters, VAS score in labour analgesia. 2)To evaluate the effect of ropivacaine and fentanyl on neonatal outcome in term of FHR, APGAR score at one and five minutes. Timepoint: 5 minutes after delivery | — |
Countries
India
Contacts
Dr. S N Medical College, Jodhpur