Evaluating sexual function in high-risk pregnant women
Evaluation of Sexual Function in High-risk Pregnant Women
This study looks at how high-risk pregnancies affect sexual health in women during their third trimester to better understand their needs.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 400 (estimated) |
| Ages | 18 Years to 40 Years |
| Sex | Female |
| Sponsor | Karabuk University Academic / other |
| Locations | 1 site (Istanbul, Sisli) |
| Trial ID | NCT06130150 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the sexual functions of pregnant women classified as high-risk, with their pregnancies monitored by perinatology specialists. The focus is on understanding how high-risk pregnancies may impact sexual health and function. By gathering data from participants in their third trimester, the study seeks to identify any correlations between pregnancy complications and sexual dysfunction. The findings could provide valuable insights into the sexual health needs of this population.
Who should consider this trial
Good fit: Ideal candidates for this study are pregnant women aged 18 to 39 years who are in their third trimester and classified as having high-risk pregnancies.
Not a fit: Patients who are under 18 years old, over 40 years old, or in their first or second trimester will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding and management of sexual dysfunction in high-risk pregnant women, leading to improved quality of life.
How similar studies have performed: While there is limited information on similar studies, the focus on sexual function in high-risk pregnancies is relatively novel and may not have been extensively tested in previous research.
Eligibility criteria
Show full inclusion / exclusion criteria
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.
Where this trial is running
Istanbul, Sisli
- Prof. Dr. Cemil Tascioglu City Hospital — Istanbul, Sisli, Turkey (Recruiting)
Study contacts
- Study coordinator: Cagdas Nurettin Emeklioglu, MD
- Email: c.n.emeklioglu@gmail.com
- Phone: +905359129913
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.