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NCT04013035 Clinical Trial

Cervical Length on Pregnancy Termination

Pregnancy Loss Clinical Trial

Official title:
The Impact of Fetal Viability and Cervical Length on Pregnancy Termination Outcomes in Nulliparous Second Trimester Pregnancies

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04013035
Other study ID # 2015.01.01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2016
Est. completion date June 1, 2017

Study information
Verified date July 2019
Source Kanuni Sultan Suleyman Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Cervical length is used as a parameter to predict cervical insufficiency and onset of labor. However, its role in predicting abortion induction is unclear.To investigate the impact of cervical length measurement and fetal viability on second trimester pregnancy termination duration in nulliparous pregnant women.

Description:

Cervical length and fetal viability were evaluated prior to second trimester pregnancy termination due to various indications. nulliparous pregnant women through 13 and 26 gestational weeks in whom pregnancy termination was conducted within 72 hours after admission were included in the study. The subjects were grouped into two groups according to fetal viability.

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date June 1, 2017
Est. primary completion date June 1, 2017
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

-Nulliparous pregnant women at 13-26 weeks of gestation

Exclusion Criteria:

- Patients with multiple gestations,

- multiparous patients or

- patients that had uterine gynecologic surgery

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• cervical length measurement
cervical length measurement at second trimester pregnancy termination in nulliparous pregnant women.

Locations
Country Name City State
Turkey Kanuni Sultan Süleyman Training and Research Hospital Istanbul

Sponsors (1)
Lead Sponsor Collaborator
Kanuni Sultan Suleyman Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary cervical length measurement cervical length measurement at second trimester pregnancy termination in nulliparous pregnant women. The measurements will be saved as a number in cm. 2 days
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