Investigating health consequences in azoospermia patients
Prospective Cohort Study for Azoospermia Patients in Clinical Reproductive Medicine Management System/Electronic Medical Record Cohort Database (CCRM/EMRCD)
This study looks at the health effects of azoospermia in men to see how it impacts their overall well-being and fertility.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 10000 (estimated) |
| Ages | 18 Years to 40 Years |
| Sex | Male |
| Sponsor | The First Affiliated Hospital of Zhengzhou University Academic / other |
| Locations | 1 site (Zhengzhou, Henan) |
| Trial ID | NCT03991663 on ClinicalTrials.gov |
What this trial studies
This observational study focuses on azoospermia, a condition affecting male fertility, by examining the short- and long-term health outcomes of affected individuals. Conducted at the Reproductive Medical Center of the First Affiliated Hospital of Zhengzhou University, the study utilizes a comprehensive database that includes biological samples, questionnaires, and health data from participants. The aim is to gather evidence that can inform prognosis and management of azoospermia, which is a significant factor in infertility for many couples.
Who should consider this trial
Good fit: Ideal candidates for this study are men diagnosed with azoospermia, confirmed by multiple semen evaluations showing no sperm.
Not a fit: Patients with azoospermia who do not meet the inclusion criteria or those with other underlying conditions affecting fertility may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the health implications of azoospermia, potentially leading to improved management strategies for affected patients.
How similar studies have performed: While there have been studies on male infertility, this specific focus on azoospermia and its health consequences is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * at least three semen evaluations performed on separate occasions, when the seminal specimen after centrifugation showed no sperm under the microscope and was then diagnosed according to several clinical parameters； Exclusion Criteria: \-
Where this trial is running
Zhengzhou, Henan
- Reproductive Medical Center, First Affiliated Hospital of Zhengzhou University — Zhengzhou, Henan, China (Recruiting)
Study contacts
- Study coordinator: Lanlan Fang, M.D.
- Email: fanglly@163.com
- Phone: 13673355291
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.