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Clinical Trial Summary

Induction of labor is performed via the vaginal misorostol 25 ug/ 6 hours and intracervical foley's cather administration and both techniques performed together.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


NCT number NCT02685085
Study type Interventional
Source Woman's Health University Hospital, Egypt
Contact Dina MR Dakhly, MD
Phone 01003498919
Email dinadakhly@gmail.com
Status Recruiting
Phase Phase 2
Start date February 2016
Completion date August 2016

See also
  Status Clinical Trial Phase
Completed NCT00468520 - Adjuvant Oxytocin for Preinduction Ripening With a Foley catheter--a Clinical Trial N/A
Completed NCT03744364 - Low-dose Vaginal Misoprostol Versus Vaginal Dinoprostone Insert for Induction of Labor Phase 4
Completed NCT01231126 - Evaluation the Blood Loss in Pregnancies With Misoprostol-induced Labour Phase 4
Terminated NCT00890630 - Intracervical Catheters for Induction of Labour in Women With Prelabour Rupture of Membranes at Term Phase 2