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Medical Errors |
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Clinical Trial: A Two Year Safety and Efficacy Study in Obese Patients
This study is not yet open for patient recruitment.
Verified by Merck August 2005
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Purpose
| Condition | Intervention | Phase |
|---|---|---|
| Obesity and obesity-related medical conditions | Drug: An investigational drug for Obesity and obesity-related medical conditions. | Phase II |
MedlinePlus consumer health information
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Eligibility
Ages Eligible for Study: 18 Years and above, Genders Eligible for Study: Both
Criteria
Inclusion Criteria:
- Obese patients with a body mass index between 30 kg/m2 and 43 kg/m2, inclusive (BMI between 27 kg/m2 and 43 kg/m2, inclusive for those with obesity-related comorbidities including hypertension, dyslipidemia, and sleep apnea.
Exclusion Criteria:Patients with serious or unstable current or past medical conditions.
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Location and Contact Information
Please refer to this study by ClinicalTrials.gov identifier NCT00131404
Toll Free Number 1-888-577-8839
Study chairs or principal investigators
Medical Monitor, Study Director, Merck
More Information
Study ID Numbers: 2005_031
Last Updated: August 17, 2005
Record first received: August 16, 2005
ClinicalTrials.gov Identifier: NCT00131404
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-08-23
Last Updated: August 17, 2005
Record first received: August 16, 2005
ClinicalTrials.gov Identifier: NCT00131404
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-08-23
Resources
- 20 Tips to Help Prevent Medical Errors (Agency for Healthcare Research and Quality Clearinghouse, AHRQ, OPHS, HHS)
- Como proteger a usted y a su familia de los errores médicos (Agency for Healthcare Research and Quality Clearinghouse, AHRQ, OPHS, HHS)
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