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Clinical Trial Summary

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


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03034434
Study type Observational [Patient Registry]
Source Rambam Health Care Campus
Contact
Status Completed
Phase
Start date March 14, 2017
Completion date June 30, 2020

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