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| Study Type: | Interventional |
|---|---|
| Study Design: | Non-Randomized, Open Label, Uncontrolled, Single Group Assignment |
| Condition: |
Diabetes Mellitus, Type 2 |
| Intervention: |
Drug: Sulfonylurea |
Participant Flow
| 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 |
| Significant events and approaches for the overall study following participant enrollment, but prior to group assignment |
|---|
| none |
| Description | |
|---|---|
| Sulfonylurea | No text entered. |
| Sulfonylurea | |
|---|---|
| STARTED | 12 |
| COMPLETED | 12 |
| NOT COMPLETED | 0 |
Baseline Characteristics
| Description | |
|---|---|
| Sulfonylurea | No text entered. |
| 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 |
Reported Adverse Events
More Information
| All Principal Investigators ARE employed by the organization sponsoring the study. |
| 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. |