Clinical Trials Directory

Trials / Completed

CompletedNCT03034434

Cervical Recuperation After Vaginal Delivery

Sonography Evaluation of Cervical Recuperation After Vaginal Delivery

Status
Completed
Phase
Study type
Observational
Enrollment
1,384 (actual)
Sponsor
Rambam Health Care Campus · Academic / Other
Sex
Female
Age
18 Years – 44 Years
Healthy volunteers
Accepted

Summary

Patients after vaginal delivery will undergo 3 trans-vaginal ultrasounds in order to examine the process of cervical recuperation post delivery.

Detailed description

Patients after vaginal delivery will be recruited after receiving a full explanation and signing an informed consent. The goal of the study is to examine cervical length after vaginal delivery at 3 different time intervals: 1. 8 hours post delivery. 2. 24 hours post delivery. 3. 48 hours post delivery. At each interval a trans-vaginal ultrasound will be performed, evaluating cervical length. At the end of the 3rd and final ultrasound, the patient will finish her participation in the study/ Information regarding obstetric conditions such as labor induction, gestational age at the time of delivery etc. will be collected from patients' electronic files.

Conditions

Interventions

TypeNameDescription
DEVICETrans-vaginal ultrasoundThree trans-vaginal ultrasounds, the 1st to be performed 8 hours post delivery, the 2nd 24 hours after delivery and the 3rd 48 hours after delivery.

Timeline

Start date
2017-03-14
Primary completion
2020-02-29
Completion
2020-06-30
First posted
2017-01-27
Last updated
2020-07-27

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT03034434. Inclusion in this directory is not an endorsement.