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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT00002276 |
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Date of registration:
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02/11/1999 |
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Primary sponsor: |
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Public title:
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The Effects of AZT and Ibuprofen on HIV-Infected Patients With Hemophilia
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Scientific title:
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Study of Bleeding Tendency, Platelet Function, and Pharmacokinetics of Azidothymidine (AZT) and Motrin (Ibuprofen) in HIV-Infected Hemophiliacs |
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Date of first enrolment:
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October 1997 |
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Target sample size:
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT00002276 |
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Study type:
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Interventional |
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Study design:
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Primary Purpose: Treatment
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Countries of recruitment
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United States
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Key inclusion & exclusion criteria
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Inclusion Criteria
Patients must have:
- Hemophilia.
- HIV-seropositivity confirmed by Western Blot.
Prior Medication:
Required:
- AZT for study patients.
Allowed:
- Ibuprofen.
Exclusion Criteria
Co-existing Condition:
Patients with the following symptoms and conditions are excluded:
Hospitalization for opportunistic infection, bacterial infection or malignancy.
Concurrent Medication:
Excluded:
- AZT (for control group).
- Antibiotics or other medication for opportunistic infection, bacterial infection, or malignancy.
Patients with the following prior conditions are excluded:
Hospitalization for opportunistic infection, bacterial infection, or malignancy.
Required:
- Ibuprofen.
- AZT 1-2 gm daily (for study patient) or not taking AZT (for control).
Age minimum:
12 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Hemophilia A
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HIV Infections
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Intervention(s)
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Drug: Ibuprofen
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Drug: Zidovudine
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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