Postpartum Sexual Function in Pregnant Women With COVID-19

Kanuni Sultan Suleyman Training and Research Hospital

Status: Completed

Conditions: COVID-19; Dyspareunia; Postpartum Period

Study type: Observational

Funder types: Other

Identifiers

NCT04389489

MTalmacCarol

Details and patient eligibility

About

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.

Enrollment: 140 patients

Sex: Female

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Pregnant Patient with COVID-19

Exclusion criteria

• Those with known sexual dysfunction disorder

Trial design

140 participants in 2 patient groups

COVID-19

Description:

Pregnant women with COVID-19 who have given birth

Control

Description:

Healthy pregnant women who have given birth