Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Conditions
Interventions
Intervention1: loading dose 50mcg of oral misoprostol followed by maintenance dose of 25mcg of vaginal misoprostol: 50 mcg misoprostol per oral
after 2 hours 25 mcg misoprostol per vaginal followed b
Sponsors
School of medical sciences and research Sharda University
Eligibility
Inclusion criteria
Inclusion criteria: 1.Nulliparity 2.POG >= 39 weeks of gestation with no associated complication 3.POG >= 34 weeks of gestation with appropriate indication for termination of pregnancy 4.Singleton pregnancy 5.Cephalic presentation 6.Assuring fetal heart rate pattern 7.Intact membranes 8.Adequate pelvis
Exclusion criteria
Exclusion criteria: 1.Mutliparity 2.Gestational age 3.Multiple pregnancies 4.H/O any uterine surgery 5.Any known hypersensitivity to misoprostol 6.Non reassuring NST 7.Ruptured membranes(PROM) & Chorioamnionitis 8.Mal-presentation 9.Patient refusal 10.Any other obstetrical, gynecological and medical contradiction to vaginal delivery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| to address clinical effectiveness (induction delivery interval and need for oxytocin) and safety (uterine tachysystole, FHR changes, meconium staining of liquor, maternal and neonatal morbidity) of proposed regimeTimepoint: from time of induction till discharge from hospital | — |
Secondary
| Measure | Time frame |
|---|---|
| 1- To study the effect on maternal and neonatal morbidity due to prolonged pregnancy. 2-To study the effect on the cesarean section rates associated with prolonged latent phase of labor. 3-To evaluate the effect of combined route on bishop score Timepoint: from time of induction till discharge from hospital | — |
Countries
India
Contacts
Public ContactDr Ruchi Srivastava
School of medical sciences and research, Sharda University
Outcome results
None listed