The Effects of AZT and Ibuprofen on HIV-Infected Patients With Hemophilia
NCT ID: NCT00002276
Last Updated: 2005-06-24
Study Results
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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COMPLETED
NA
INTERVENTIONAL
Brief Summary
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Detailed Description
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Conditions
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Study Design
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TREATMENT
Interventions
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Ibuprofen
Zidovudine
Eligibility Criteria
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Inclusion Criteria
* Hemophilia.
* HIV-seropositivity confirmed by Western Blot.
Prior Medication:
Required:
\- AZT for study patients.
Allowed:
\- Ibuprofen.
Exclusion Criteria
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).
12 Years
ALL
No
Sponsors
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University of Pittsburgh
OTHER
Locations
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Hemophilia Ctr of Western PA / Univ of Pittsburgh
Pittsburgh, Pennsylvania, United States
Countries
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References
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Ragni MV, Miller BJ, Whalen R, Ptachcinski R. Bleeding tendency, platelet function, and pharmacokinetics of ibuprofen and zidovudine in HIV(+) hemophilic men. Am J Hematol. 1992 Jul;40(3):176-82. doi: 10.1002/ajh.2830400305.
Other Identifiers
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044A
Identifier Type: -
Identifier Source: org_study_id