Clinical Trials Directory

Trials / Completed

CompletedNCT04454346

Double Foley Catheter For Cervical Ripening

Double Foley Catheter For Ripening The Unfavorable Cervix: An Alternative Method

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
222 (actual)
Sponsor
Etlik Zubeyde Hanım Women's Health Care, Training and Research Hospital · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

To compare the efficacy of three mechanical devices for pre-induction of labour cervical ripening: the Single Foley Catheter, Double Foley Catheter (a new handmade device) and Cook cervical ripening balloon.

Detailed description

This prospective study Scheduled included 74 Double Foley Catheter, 74 Single Foley catheter group and 74 Cook cervical ripening catheter group. All pregnant women will be randomly allocated into three groups: the single Foley, Double Foley Catheter or Cook balloon catheter. Removal of the catheters is planned approximately 12 h after insertion if spontaneous expulsion occurred. The main outcome measures include changes in Bishop score, insertion to delivery time, mode of delivery and occurrence of adverse effects. Double Foley Catheter is a new method for cervical ripening that Two 18-Fr Foley catheters are connected with sterile suture from the hole end and where the balloons borders end. Both catheters are pushed above the internal cervical os the uterus. One of 18-Fr Foley catheter full with 80 mL of normal saline. The other Foley catheter is pulled into the vagina by applying traction and full with 80 mL of normal saline. The cervix between two balloons of Foley catheters exposed to pressure from both sides from the Foley catheter's balloon's similar to Cook balloon.

Conditions

Interventions

TypeNameDescription
DEVICEDouble Foley Catheter For Ripening The Unfavorable CervixNew method

Timeline

Start date
2020-07-15
Primary completion
2020-11-01
Completion
2020-11-15
First posted
2020-07-01
Last updated
2022-01-12

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT04454346. Inclusion in this directory is not an endorsement.