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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00624624
Other study ID # LTC-472-120607
Secondary ID
Status Completed
Phase N/A
First received February 15, 2008
Last updated November 5, 2014
Start date September 2009
Est. completion date March 2011

Study information

Verified date November 2014
Source Rijnstate Hospital
Contact n/a
Is FDA regulated No
Health authority Netherlands: Dutch Health Care Inspectorate
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine the natural course of the androgen profile after bariatric surgery in men with obesity related hypogonadotropic hypogonadism.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date March 2011
Est. primary completion date March 2011
Accepts healthy volunteers No
Gender Male
Age group 20 Years to 55 Years
Eligibility Inclusion Criteria:

- Male

- Age 20-55 years

- Planned bariatric procedure

- Helicobacter pylori negative or adequate HP eradication

Exclusion Criteria:

- Liver and/or kidney dysfunction

- Psychiatric disease

- Medication influencing androgen profile and/or bone metabolism

- Weight > 160 kg

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Netherlands Rijnstate Hospital Arnhem

Sponsors (1)

Lead Sponsor Collaborator
Rijnstate Hospital

Country where clinical trial is conducted

Netherlands, 

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