Premature Rupture of Mambrane and Unfavourable Cervix

• Status: Unknown status
• Trial end date: 2014-07-01
• Target enrollment: 0
• Participant gender: Female

Summary

The paucity of published data concerning the issue of mechanical labor induction in the setting of Term PROM has led us to undertake the present clinical trial. This study is designed to compare the efficacy and safety of the standard Oxytocin induction protocol with the double-balloon catheter device with concurrent oxytocin administration in patients with Term PROM and unfavorable cervical conditions.

• Phase: N/A
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Hillel Yaffe Medical Center
• Treatments: Oxytocin

Criteria

Inclusion Criteria:

1. Diagnosed to be pregnant with PROM at > 34 week

2. Found to have a Bishop score of 4 points or less.

3. Diagnosed as having a singleto

4. Willingness to comply with the protocol for the duration of the study.

5. Have signed an informed consent.

Exclusion Criteria:

1. Any contraindication for a vaginal deliver

2. Regular uterine contractn

3. Evidence of chorio-amonitis

4. Previous cesarean section or presence of any uterine scar.

5. Suspected placental abruption or presence of a significant hemorrhage.

6. Non-reassuring fetal statu