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Clinical Trial Summary

A randomised controlled trial comparing cervical ripening using foley catheter as in- or outpatient setting.


Clinical Trial Description

The study evaluated the efficacy and safety of outpatient versus inpatient Foley catheter cervical ripening and patients' satisfaction. Sixty low-risk women were randomized to outpatient and inpatient management of intracervical Foley catheter digital insertion. The outpatient group was provided with verbal and written 24-hours contact information and instructions. Both groups were reassessed the next morning unless labor had begun or the catheter had dropped off. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04342741
Study type Interventional
Source National University of Malaysia
Contact
Status Completed
Phase N/A
Start date August 1, 2017
Completion date May 31, 2018