- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00253253
Long-Term Outcome in Congenital Undescended Testis After Surgical Treatment by Orchidopexy
May 21, 2008 updated by: Medical Center Alkmaar
The purpose of this study is to determine the long-term outcome in congenital undescended testis after surgical treatment by orchidopexy and to what extent orchidopexy is the treatment for congenital undescended testis.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
181
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Noord-Holland
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Alkmaar, Noord-Holland, Netherlands, 1815 J D
- Medical Center Alkmaar
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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
6 months to 25 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- The orchidopexy has taken place in the Medical Center Alkmaar between 1986-2004
- The indication concerned a congenital undescended testis
- It concerns a first orchidopexy to the concerning testis
Exclusion Criteria:
- Orchidopexy has taken place on an other reason than congenital undescended testis (for example: torsio testis)
- It concerns re-orchidopexy
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.W. M. Hack, MD, PhD, Department of Pediatrics, Medical Centre Alkmar
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
August 1, 2006
Study Completion
January 1, 2007
Study Registration Dates
First Submitted
November 14, 2005
First Submitted That Met QC Criteria
November 14, 2005
First Posted (Estimate)
November 15, 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
Additional Relevant MeSH Terms
Other Study ID Numbers
- P05.936L
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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