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NCT04389489 Clinical Trial

Postpartum Sexual Function in Pregnant Women With COVID-19

COVID-19 Clinical Trial

Official title:
Evaluation of Pregnant Women Diagnosed With COVID-19 Using Carol Postpartum Sexual Function and Dyspareunia Scale

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04389489
Other study ID # MTalmacCarol
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 14, 2020
Est. completion date September 30, 2020

Study information
Verified date March 2023
Source Kanuni Sultan Suleyman Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to identify women with postpartum sexual dysfunction and dyspareunia risk in the early period and to use the treatment and care services they need effectively. Our secondary aim is to reveal the difference in sexual life in the postpartum period between healthy pregnant women and pregnant women diagnosed with COVID-19.

Recruitment information / eligibility
Status Completed
Enrollment 140
Est. completion date September 30, 2020
Est. primary completion date September 25, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Pregnant Patient with COVID-19 Exclusion Criteria: - Those with known sexual dysfunction disorder

Study Design

Related Conditions & MeSH terms

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

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

Country where clinical trial is conducted

Turkey, 

References & Publications (1)

Lopez-Lapeyrere C, Serna-Gomez N, Hernandez-Lopez AB, Perez-Garcia MF, Tejeda-Esteban A, Solis-Munoz M. The development and validation of a new postpartum sexual function and dyspareunia assessment tool: The Carol Scale. Midwifery. 2018 Mar;58:27-36. doi: 10.1016/j.midw.2017.11.008. Epub 2017 Dec 6. — View Citation

Outcome
Type Measure Description Time frame Safety issue
Primary Evaluation of pregnant women diagnosed with COVID-19 using Carol Postpartum Sexual Function and Dyspareunia Scale In the study planned to be carried out, it is aimed to identify women at risk of postpartum sexual dysfunction and dyspareunia early and benefit from the treatment and care services they need effectively. 3 months
Secondary Evaluation of pregnant women diagnosed with COVID-19 using Carol Postpartum Sexual Function and Dyspareunia Scale To reveal the difference in sexual life in postpartum period between healthy pregnant women and pregnant women diagnosed with COVID-19. 3 Months
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