- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00264121
The Incidence of Congenital Undescended Testis Among Dutch Infants
May 21, 2008 updated by: Medical Center Alkmaar
The Incidence of Congenital Undescended Testis Among Dutch Infants in the Medical Centre Alkmaar
The purpose of this study is to determine the incidence of congenital undescended testis of mature boys, at one year of age, born in the Medical Centre Alkmaar (MCA).
Study Overview
Status
Unknown
Conditions
Detailed Description
The position of the testes of mature boys will be registered at birth and boys with a high-scrotal, non-scrotal or dubious position of the testis/ testes will be followed up (till the age of one year).
Study Type
Observational
Enrollment (Anticipated)
3000
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: K. Sijstermans, MD
- Phone Number: +31-72-5482998
- Email: k.sijstermans@mca.nl
Study Contact Backup
- Name: W WM Hack, PhD
- Phone Number: +31-72-5484444
- Email: w.hack@mca.nl
Study Locations
-
-
Noord-Holland
-
Alkmaar, Noord-Holland, Netherlands
- Recruiting
- Medical Center Alkmaar (MCA)
-
Contact:
- K Sijstermans, MD
- Phone Number: +31-72-5482998
- Email: k.sijstermans@mca.nl
-
-
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
No older than 1 year (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- mature newborns (>/= 37 weeks)
- born in the Medical Centre Alkmaar
Exclusion Criteria:
- premature newborns (< 37 weeks)
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
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: W WM Hack, PhD, Department of Pediatrics, Medical Centre Alkmaar
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
June 1, 2005
Study Completion
June 1, 2008
Study Registration Dates
First Submitted
December 9, 2005
First Submitted That Met QC Criteria
December 9, 2005
First Posted (Estimate)
December 12, 2005
Study Record Updates
Last Update Posted (Estimate)
May 22, 2008
Last Update Submitted That Met QC Criteria
May 21, 2008
Last Verified
May 1, 2008
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- P05.0318L
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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