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Erectile Dysfunction and Diabetes Mellitus

This study has been completed.
Sponsor:
Information provided by:
University Hospital, Ghent
ClinicalTrials.gov Identifier:
NCT00134329
First received: August 23, 2005
Last updated: December 19, 2007
Last verified: December 2007

August 23, 2005
December 19, 2007
May 2005
Not Provided
  • Documentation of the prevalence of erectile dysfunction in the diabetic convention
  • Increase the awareness of diabetologist for erectile dysfunction
  • Relation of erectile dysfunction with metabolic parameters
  • Relation of erectile dysfunction with sex steroids
  • Documentation of the prevalence of erectile dysfunction in the diabetic convention
  • Increase the awareness of diabetologist for erectile dysfunction
  • Relation of erectile dysfunction with metabolic parameters
  • Relation of erectile dysfunction with sex steroids
Complete list of historical versions of study NCT00134329 on ClinicalTrials.gov Archive Site
  • Adjustment of the systematic follow-up of diabetic complications.
  • Optimalisation of the healthcare for diabetic patients, so that the quality of life for male diabetic patients can be improved
  • Adjustment of the systematic follow-up of diabetic complications.
  • Optimalisation of the healthcare for diabetic patients, so that the quality of life for male diabetic patients can be improved
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Not Provided
 
Erectile Dysfunction and Diabetes Mellitus
Erectile Dysfunction and Diabetes Mellitus

This study consists of filling out a questionnaire on possible erectile dysfunction.

Male diabetic patients who attend a diabetic routine year program visit will be asked to give their voluntary permission to fill out a questionnaire on possible erectile dysfunction.

The questionnaire consists of two parts: Part 1 is the IIEF (International Index of Erectile Function) questionnaire and Part 2 is an additional questionnaire. The included patients have to fill out these questionnaires two times; once at the beginning at a diabetic year program visit and a second time one year later at the next diabetic year program consultation.

The patients will also be asked to give their permission for using their results of the routine diabetic year program for scientific research.

Observational
Time Perspective: Prospective
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Not Provided
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  • Diabetes Mellitus
  • Erectile Dysfunction
Procedure: Filling out a questionnaire on the possible occurrence of erectile dysfunction
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
300
March 2007
Not Provided

Inclusion Criteria:

  • Male diabetic patients
  • Age older than 18 years

Exclusion Criteria:

Male
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Belgium
 
NCT00134329
2005/096
No
Not Provided
University Hospital, Ghent
Not Provided
Principal Investigator: Guy T'Sjoen, MD University Hospital, Ghent
University Hospital, Ghent
December 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP