Skip to main content
MedPathMedPath Home
Clinical Trials/CTRI/2019/06/019821
CTRI/2019/06/019821
Not yet recruiting
Phase 4

To Study The Effect of Oral Mifepristone as an Adjunct to Other Methods of Pre-induction Cervical Ripening in Term Pregnancy â?? A Randomized Controlled trial

Paily V P0 sites0 target enrollmentTBD
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
ConditionsHealth Condition 1: O80- Encounter for full-term uncomplicated delivery

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Sponsor
Paily V P
Status
Not yet recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Paily V P

Eligibility Criteria

Inclusion Criteria

  • •A. Primigravida singleton pregnancy at or more than 39 weeks gestation with cephalic presentation and intact membranes and no complications other than Gestational Diabetes Mellitus.
  • •B. Modified Bishop Score less than 6\.
  • •C. Patient should not have any contraindications for vaginal delivery

Exclusion Criteria

  • •A. Multi\-parity
  • •B. Multiple pregnancy
  • •C. Premature rupture of Membranes
  • •D. Previous Cesarean Section
  • •E. Scarred uterus
  • •F. Uterine Anomalies
  • •G. Malpresentations
  • •H. Bad Obstetric History
  • •I. Cephalo\-pelvic Disproportion, Short Primi (height \<145cm)
  • •J. Indicated Induction for Gestational Hypertension, overt Diabetes and Gestational

Outcomes

Primary Outcomes

Not specified

Similar Trials

Completed
Not Applicable
Study comparing two methods of abortion in second trimester using misoprostol or ethacridine lactate after priming with mifepristoneHealth Condition 1: null- SECOND TRIMESTER ABORTIONS
CTRI/2018/01/011157Project in the Department of Obstetrics and Gynecology120
Not yet recruiting
Not Applicable
To study the effect of tablet Mifepristone (200 mg) in induction of labour in term pregnancy in a tertiary care hospital at chengalpatu district.Health Condition 1: O80- Encounter for full-term uncomplicated delivery
CTRI/2024/03/064272Thiripurasundari
Completed
Not Applicable
The effect of daily low dose mifepristone on the endometrium - study over four consecutive cyclesObstetrics and gynaecologyPregnancy and Childbirth
ISRCTN88271422Medical Research Council (MRC) (UK)40
Not yet recruiting
Not Applicable
Trial of induction of labour by oral drug in late intrauterine fetal death
CTRI/2023/06/053692none
Completed
Not Applicable
The effect of a single dose of mifepristone given midcycle on the pattern of menstrual bleedingObstetrics and gynaecology: Menstrual bleedingUrological and Genital DiseasesObstetrics and gynaecology
ISRCTN23968812niversity of Edinburgh (UK)400