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Postpartum Sexual Function in Pregnant Women With COVID-19

NCT04389489 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 140

Last updated 2023-03-30

No results posted yet for this study

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.

Conditions

  • COVID-19
  • Dyspareunia
  • Postpartum Period

Sponsors & Collaborators

  • Kanuni Sultan Suleyman Training and Research Hospital

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-05-14
Primary Completion
2020-09-25
Completion
2020-09-30

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04389489 on ClinicalTrials.gov