The Percentage of Cases of Acute Treatment With Allopurinol in Gout Patients

NCT ID: NCT03601260

Last Updated: 2018-07-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

700 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-08-31

Study Completion Date

2018-12-31

Brief Summary

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The aim of the study is to determine the percentage of cases of acute treatment with Allopurinol in gout patients who have been previously treated.

Detailed Description

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Conditions

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Gout

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Gout Patients

Allopurinol 100 mg-300mg/day as secondary treatment in gout patients

Group Type OTHER

Allopurinol

Intervention Type DRUG

Treatment of gout patients by oral dosage of 100 mg-300mg/ day of Allopurinol

Interventions

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Allopurinol

Treatment of gout patients by oral dosage of 100 mg-300mg/ day of Allopurinol

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Gout patients

Exclusion Criteria

* Pregnant women
* Chronic renal failure
* Patients with Allopurinal hypersensitivity
Minimum Eligible Age

25 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hillel Yaffe Medical Center

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Hillel Yaffe Medical Center

Hadera, , Israel

Site Status

Countries

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Israel

Central Contacts

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Fadi Khalaila, MD

Role: CONTACT

972-52-3326629

Facility Contacts

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Fadi Khalaila, MD

Role: primary

972-52-3326629

Other Identifiers

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HYMC-FKH-1

Identifier Type: -

Identifier Source: org_study_id

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