- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02267252
Effects of Male-specific Antibodies on Sex Ratio
November 1, 2023 updated by: Jens Fedder, Odense University Hospital
Investigation of the ability of antibodies from vasectomized men in binding to Y-spermatozoa as a possible explanation of the lower sex ratio observed after microinsemination using epididymal sperm from vasectomized men.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jens Fedder, MD, PhD
- Phone Number: +45 26820368
- Email: fedder@dadlnet.dk
Study Locations
-
-
-
Odense, Denmark, 5000
- Recruiting
- Fertility Clinic, Odense University Hospital
-
Contact:
- Jens Fedder, Professor
- Phone Number: +45 268 20 368
- Email: fedder@dadlnet.dk
-
Principal Investigator:
- Jens Fedder, Professor
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
25 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Vasectomized men
Description
Inclusion Criteria:
- Vasectomized men
Exclusion Criteria:
- Men who do not understand the study information
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Y/X sperm ratio after exposure to sperm-specific antibodies
Time Frame: Up to 28 months
|
Up to 28 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 1, 2014
Primary Completion (Estimated)
December 1, 2024
Study Completion (Estimated)
June 1, 2025
Study Registration Dates
First Submitted
October 8, 2014
First Submitted That Met QC Criteria
October 14, 2014
First Posted (Estimated)
October 17, 2014
Study Record Updates
Last Update Posted (Actual)
November 2, 2023
Last Update Submitted That Met QC Criteria
November 1, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Lab.Reprod.Biol.- Odense.01
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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