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The Beta Cell Responsiveness to Glucose-Dependent Insulinotropic Polypeptide (GIP) With and Without Sulfonylurea in Patients With Type 2 Diabetes
This study has been completed.
Study NCT00321321.   Last updated on October 1, 2008.
Information provided by University Hospital, Gentofte, Copenhagen
Study Type: Interventional
Study Design: Non-Randomized, Open Label, Uncontrolled, Single Group Assignment
Condition: Diabetes Mellitus, Type 2
Intervention: Drug: Sulfonylurea


  Participant Flow
Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
May 2006 - March 2007, Outpatient clinic and advertisement

Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
none

Reporting Groups
  Description
Sulfonylurea No text entered.

Participant Flow:   Overall Study
  Sulfonylurea
STARTED   12  
COMPLETED   12  
NOT COMPLETED   0  





  Baseline Characteristics
Reporting Groups
  Description
Sulfonylurea No text entered.

Baseline Measures
  Sulfonylurea
Number of Participants  
[units: participants]
12
Age  
[units: participants]
 
<=18 years 0
Between 18 and 65 years 11
>=65 years 1
Age  
[units: years]
Mean ± Standard Deviation
55 ± 7.6
Gender  
[units: participants]
 
Female 4
Male 8
Region of Enrollment  
[units: participants]
 
Denmark 12





  Outcome Measures

1.   Primary Outcome Measure:   Insulin Secretion




  Reported Adverse Events
Adverse event information has not been entered for this trial.

The submission of adverse events information is currently optional and is not mandated under U.S. Federal Law (US Public Law 110-85, Title VIII) until September 27, 2009.




  More Information
Certain Agreements:  
All Principal Investigators ARE employed by the organization sponsoring the study.


Limitations and Caveats
Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
No text entered.  


Results Point of Contact:  
Name/Title: Dr. Kasper Aaboe
Organization: Gentofte Hospital, University of Copenhagen
phone: +4539978474
e-mail: Kasper@dadlnet.dk


Responsible Party:
Gentofte University Hospital ( Kasper Aaboe )
Study ID Numbers:
KA-05011
Study First Received:
May 2, 2006
Results First Received:
September 29, 2008
Last Updated:
October 1, 2008
ClinicalTrials.gov Identifier:
NCT00321321
Health Authority:
Denmark: Ethics Committee