- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00907881
The OBSTACLE Hypoglycemia Study (MK-0000-158)
April 1, 2015 updated by: Merck Sharp & Dohme LLC
Prospective Observational Study to Assess Correlation Between Glycemic Control and Hypoglycemia in Patients With Type 2 Diabetes Treated With Sulfonylurea
This study will assess the correlation between glycemic control and the hypoglycemia symptom score in patients with Type 2 diabetes, 12 weeks after addition of a sulfonylurea to an ongoing regime of oral hypoglycemic agents.
Study Overview
Detailed Description
Patients will be evaluated for participation in the study during their usual visit to participating diabetes care clinics.
Addition of sulfonylurea will be an unbiased decision of the participating physicians based on the clinical needs of the participating patients.
Study Type
Observational
Enrollment (Actual)
1069
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
18 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Diabetic clinic patients
Description
Inclusion Criteria:
- Patients with Type 2 Diabetes, of either gender and aged between 18-75 years
- Patients being considered for addition of Sulfonylurea on background of at least one other oral hypoglycemic agent, on a usual visit (screening cum enrolment visit), as per the clinical situation judged by participating physician
- Willing to comply with study requirements
Exclusion Criteria:
- Patients with type 1 Diabetes or gestational Diabetes
- Patients currently on insulin therapy or have received Insulin in last 6 months
- Patients currently on Sulfonylurea therapy or have received Sulfonylureas in last 6 months
- Patients currently on Meglitinides therapy or have received Meglitinides in last 6 months
- Patients initiated on Sulfonylurea monotherapy
- Patient on DPP-4 inhibitors, either as monotherapy or as combination therapy
- Patient is, at the time of signing informed consent, a user of recreational or illicit drugs or has had a recent history (within the last year) of drug or alcohol abuse or dependence.
- Patients for whom it would be impossible to complete the questionnaire for whatever reason, in any feasible form
- Patients who are already participating in a clinical trial or other clinical study
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
All participants
Participants with type 2 diabetes mellitus (T2DM) who had sulfonylurea treatment added to an on-going regime of oral hypoglycemic agent(s).
|
The dose and frequency of administration of study drug (sulfonylurea) was decided by the investigator according to the individual need of each participant.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Correlation Between HbA1c Values at Week 12 and Hypoglycemia Scores
Time Frame: Week 12
|
Coefficient of correlation was measured using a linear regression analysis for the association between two variables, HbA1c values at Week 12 and hypoglycemia scores.
A negative correlation coefficient indicates that as one value increases the other value decreases, and vice versa.
|
Week 12
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hypoglycemia Symptom Score by Sub-group (Demographic/Disease Parameters)
Time Frame: Week 12
|
Sub-group analyses of mean hypoglycemia symptom score.
Participants were grouped based on gender, age, hypoglycemia severity, body mass index, duration of diabetes, and number of oral hypoglycemic agents.
Hypoglycemia symptom score (measured by Stanford Hypoglycemia Questionnaire) is a score on a scale with a possible range of 0 (best) to 7 (worst).
The questionnaire was administered by the physician at Week 12.
|
Week 12
|
Correlation Between HbA1c Values at Week 12 and Hypoglycemia Scores by Sub-group (Demographic/Disease Parameters)
Time Frame: Week 12
|
Sub-group analyses based on Karl pearson coefficient of correlation for HbA1c values at Week 12 and hypoglycemia score.
Participants were grouped based on gender, age, body mass index, and duration of diabetes.
A negative correlation coefficient indicates that as one value increases the other value decreases, and vice versa.
|
Week 12
|
Correlation Between HbA1c Values at Baseline and Hypoglycemia Scores at Week 12
Time Frame: Baseline and Week 12
|
Coefficient of correlation as measured using linear regression analysis for association between two variables, HbA1c values at baseline and hypoglycemia scores.
A positive correlation coefficient indicates that as one value increases the other value increases, or as as one value decreases the other value decreases.
|
Baseline and Week 12
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Kalra S, Deepak MC, Narang P, Singh V, Uvaraj MG, Agrawal N. Usage pattern, glycemic improvement, hypoglycemia, and body mass index changes with sulfonylureas in real-life clinical practice: results from OBSTACLE Hypoglycemia Study. Diabetes Technol Ther. 2013 Feb;15(2):129-35. doi: 10.1089/dia.2012.0237. Epub 2013 Jan 5.
- Kalra S, Deepak MC, Narang P, Singh V, Maheshwari A. Correlation between measures of hypoglycemia and glycemic improvement in sulfonylurea treated patients with type 2 diabetes in India: results from the OBSTACLE hypoglycemia study. J Postgrad Med. 2014 Apr-Jun;60(2):151-5. doi: 10.4103/0022-3859.132322.
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, 2009
Primary Completion (Actual)
May 1, 2010
Study Completion (Actual)
May 1, 2010
Study Registration Dates
First Submitted
May 21, 2009
First Submitted That Met QC Criteria
May 22, 2009
First Posted (Estimate)
May 25, 2009
Study Record Updates
Last Update Posted (Estimate)
April 21, 2015
Last Update Submitted That Met QC Criteria
April 1, 2015
Last Verified
April 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0000-158
- 2009_001
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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