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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01775098
Other study ID # Allopurinol in acute gout
Secondary ID
Status Withdrawn
Phase N/A
First received January 21, 2013
Last updated May 10, 2017
Est. completion date February 2013

Study information

Verified date May 2017
Source Université de Sherbrooke
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date February 2013
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
allopurinol
No arms will not be change as the study as been closed.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Université de Sherbrooke

Outcome

Type Measure Description Time frame Safety issue
Primary Duration of the gout crises Presence of inflammatory signs First 7 days after visit
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