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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06130150
Other study ID # KBU-EMEKLIOGLU-002
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 10, 2021
Est. completion date January 2024

Study information

Verified date November 2023
Source Karabuk University
Contact Cagdas Nurettin Emeklioglu, MD
Phone +905359129913
Email c.n.emeklioglu@gmail.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Our aim with this study is to evaluate the sexual functions of pregnant women whose pregnancies are defined as high-risk pregnancies and whose pregnancies are followed by perinatology specialists.


Recruitment information / eligibility

Status Recruiting
Enrollment 400
Est. completion date January 2024
Est. primary completion date January 10, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - Pregnant women over 18 years old, -Pregnant women 39 years old and under, -Pregnant women in their 3rd trimester. Exclusion Criteria: - Pregnant women under 18 years old, -Pregnant women over 40 years old, -Pregnant women in their 1st or 2nd trimester.

Study Design


Locations

Country Name City State
Turkey Prof. Dr. Cemil Tascioglu City Hospital Istanbul Sisli

Sponsors (1)

Lead Sponsor Collaborator
Karabuk University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary 1 High-risk pregnant women have lower FSFI score results then normal pregnant women 1 day
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