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comparision of two drugs,used to initiate labour

Not Applicable
Conditions
Health Condition 1: O619- Failed induction of labor, unspecified
Registration Number
CTRI/2021/10/037559
Lead Sponsor
Shri BM Patil Medical College
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Singleton pregnancy

2.Cephalic presentation

3.BISHOP SCORE <6

4.Post maturity

5.FGR

6.Oligohydromnios and polyhydromnios

7.Rh isoimmunization

8.Premature rupture of membranes

9.IUD

Exclusion Criteria

1.Absolute contracted pelvis and cephalopelvic disproportion

2.Pre Existing Cardiac Disorders

3.Malpresentation (breech,transverse,oblique lie)

4.Previous lscs or hysterotomy

5.Vasa previa,placenta previa

6.Acute genital herpes.

7.umbilical cord prolapse

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
THE MAIN OUTCOME MEASURES RECORDED ARE:INDUCTION TO ACTIVE LABOUR INTERVAL <br/ ><br>BISHOPS SCORE <br/ ><br>1.On admission: <br/ ><br> <br/ ><br>2.After induction: <br/ ><br>AUGMENTATION WITH OXYTOCIN OR ARM <br/ ><br>INDUCTION TO DELIVERY INTERVAL <br/ ><br>COLOR OF LIQOUR <br/ ><br> <br/ ><br>. MODE OF DELIVERY: <br/ ><br>â?¢Vaginal delivery: <br/ ><br>â?¢Instrumental delivery: <br/ ><br>â?¢LSCS: Indication: <br/ ><br> <br/ ><br>9.PERINATAL OUTCOME: <br/ ><br>â?¢Mother side: <br/ ><br>â?¢NICU: <br/ ><br>â?¢Mortality <br/ ><br>Timepoint: 4hrs,6hrs,12hrs.
Secondary Outcome Measures
NameTimeMethod
To Evaluate the efficacy and safety of sublingual misoprostol vs intracervical dinoprostone gel for induction of labour <br/ ><br>Timepoint: neonatal outcome after 24hours
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