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| Tracking Information | |||||
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| First Received Date ICMJE | February 14, 2008 | ||||
| Last Updated Date | March 4, 2008 | ||||
| Start Date ICMJE | September 2007 | ||||
| Primary Completion Date | February 2008 (final data collection date for primary outcome measure) | ||||
| Current Primary Outcome Measures ICMJE |
Increased base line creatinine at least 25% [ Time Frame: 24 hr later ] [ Designated as safety issue: No ] | ||||
| Original Primary Outcome Measures ICMJE | Same as current | ||||
| Change History | Complete list of historical versions of study NCT00634491 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE | |||||
| Original Secondary Outcome Measures ICMJE | |||||
| Descriptive Information | |||||
| Brief Title ICMJE | Comparison Between Effect of Acetazolamide and NaHco3 in Prevention of Contrast Nephropathy | ||||
| Official Title ICMJE | Effect of Acetazolamide in Prevention of Contrast Nephropathy | ||||
| Brief Summary | The purpose of this study is whether Acetazolamide is effective in prevention of contrast nephropathy |
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| Detailed Description | Contrast induced nephropathy is one of common causes of acute renal failure many preventive protocol existed . 240 patient that underwent coronary angiography randomly divided in three groups.Group 1,2,3 will receive Bicarbonate ,Acetazolamide+Normal salin and Normal salin respectively.We compare prevalence of contrast nephropathy in each group. |
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| Study Phase | Phase II | ||||
| Study Type ICMJE | Interventional | ||||
| Study Design ICMJE | Prevention, Randomized, Double Blind (Subject, Investigator), Active Control, Parallel Assignment | ||||
| Condition ICMJE | Contrast Induced Nephropathy | ||||
| Intervention ICMJE |
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| Study Arms / Comparison Groups |
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| Publications * | Assadi F. Acetazolamide for prevention of contrast-induced nephropathy: a new use for an old drug. Pediatr Cardiol. 2006 Mar-Apr;27(2):238-42. | ||||
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* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Completed | ||||
| Enrollment ICMJE | 240 | ||||
| Completion Date | February 2008 | ||||
| Primary Completion Date | February 2008 (final data collection date for primary outcome measure) | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 18 Years to 80 Years | ||||
| Accepts Healthy Volunteers | Yes | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | Iran, Islamic Republic of | ||||
| Administrative Information | |||||
| NCT ID ICMJE | NCT00634491 | ||||
| Responsible Party | Office of Vice Chancellor for research in Shiraz UMS, Shiraz University of Medical Science | ||||
| Study ID Numbers ICMJE | 2438 | ||||
| Study Sponsor ICMJE | Shiraz University of Medical Sciences | ||||
| Collaborators ICMJE | Fars Heart Foundation | ||||
| Investigators ICMJE |
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| Information Provided By | Shiraz University of Medical Sciences | ||||
| Verification Date | March 2008 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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