Study Stopped
because of a lack of funding
Allopurinol in Acute Gout
1 other identifier
interventional
N/A
0 countries
N/A
Brief Summary
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
Trial Health
Trial Relationships
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Study Timeline
Key milestones and dates
Primary Completion
Last participant's last visit for primary outcome
December 1, 2012
CompletedFirst Submitted
Initial submission to the registry
January 21, 2013
CompletedFirst Posted
Study publicly available on registry
January 24, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2013
CompletedMay 11, 2017
May 1, 2017
January 21, 2013
May 10, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Duration of the gout crises
Presence of inflammatory signs
First 7 days after visit
Study Arms (2)
Allopurinol
EXPERIMENTALtreatment with allopurinol
placebo
PLACEBO COMPARATORplacebo comparator
Interventions
Eligibility Criteria
You may qualify if:
- More than 18 years old Able to sign informed consent Indication of long-term treatment with allopurinol Acute gout crisis
You may not qualify if:
- Les than 18 years-old Unable to consent Contra-indication to allopurinol
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Doctor
Study Record Dates
First Submitted
January 21, 2013
First Posted
January 24, 2013
Primary Completion
December 1, 2012
Study Completion
February 1, 2013
Last Updated
May 11, 2017
Record last verified: 2017-05