Allopurinol in Acute Gout
This study has been withdrawn prior to enrollment.
(because of a lack of funding)
Sponsor:
Universitaire de Sherbrooke
Information provided by (Responsible Party):
Artur de Brum-Fernandes, Universitaire de Sherbrooke
ClinicalTrials.gov Identifier:
NCT01775098
First received: January 21, 2013
Last updated: NA
Last verified: January 2013
History: No changes posted
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Purpose
The objectives of the present study are to determine if starting treatement of hyperuricemia with allopurinol during an acute gout crises has an impact on the duration or the severity of the crises
| Condition | Intervention |
|---|---|
|
Gout |
Drug: allopurinol |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator) Primary Purpose: Treatment |
| Official Title: | Allopurinol in Acute Gout |
Resource links provided by NLM:
Further study details as provided by Universitaire de Sherbrooke:
Primary Outcome Measures:
- Duration of the gout crises [ Time Frame: First 7 days after visit ] [ Designated as safety issue: No ]Presence of inflammatory signs
| Enrollment: | 0 |
| Estimated Primary Completion Date: | April 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Allopurinol
treatment with allopurinol
|
Drug: allopurinol |
|
Placebo Comparator: placebo
placebo comparator
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
More than 18 years old Able to sign informed consent Indication of long-term treatment with allopurinol Acute gout crisis
Exclusion Criteria:
Les than 18 years-old Unable to consent Contra-indication to allopurinol
Contacts and Locations
No Contacts or Locations Provided
More Information
No publications provided
| Responsible Party: | Artur de Brum-Fernandes, Doctor, Universitaire de Sherbrooke |
| ClinicalTrials.gov Identifier: | NCT01775098 History of Changes |
| Other Study ID Numbers: | Allopurinol in acute gout |
| Study First Received: | January 21, 2013 |
| Last Updated: | January 21, 2013 |
| Health Authority: | Canada: Health Canada |
Keywords provided by Universitaire de Sherbrooke:
|
Gout uric acid allopurinol |
Additional relevant MeSH terms:
|
Gout Arthritis Joint Diseases Musculoskeletal Diseases Rheumatic Diseases Purine-Pyrimidine Metabolism, Inborn Errors Metabolism, Inborn Errors Genetic Diseases, Inborn Metabolic Diseases Allopurinol Enzyme Inhibitors |
Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Gout Suppressants Antirheumatic Agents Therapeutic Uses Free Radical Scavengers Antioxidants Antimetabolites Protective Agents Physiological Effects of Drugs |
ClinicalTrials.gov processed this record on May 19, 2013