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Trial NCT00000662

Resource URI: http://static.linkedct.org/resource/trials/NCT00000662
PropertyValue
linkedct:brief_title A Treatment IND for Retrovir Brand Zidovudine (AZT) Therapy of Pediatric Patients With HIV Disease
linkedct:collaborator_agency <http://static.linkedct.org/resource/collabagency/3124>
linkedct:condition <http://static.linkedct.org/resource/condition/5486>
linkedct:criteria Inclusion Criteria Concurrent Treatment: Allowed: - Blood transfusions for hematologic toxicity. Criteria for children 3 months to less than 15 months of age: - Patient must be HIV antibody-positive by repeated reactive screening test (e.g., ELISA) and positive confirmatory test (e.g., Western blot). OR - If antibody-negative, patient must have two positive p24 antigen determinations performed at least one week apart or have had a positive HIV culture. Patients must meet two of the following criteria: - Be HIV culture positive or p24 antigen positive. - Have at least one of the Class P-2 symptoms (by CDC criteria). Be immunosuppressed defined as having: - CD4+(T4) lymphocytes = or < 400 cells/mm3. - Abnormal age adjusted immunoglobulin levels (IgG or IgA). Decreased helper/suppressor ratio < 1.0. Note: - In general, abnormal values for any of the above lab tests should be confirmed in 2 measurements at least 1 week apart, and other clinical causes for these abnormalities should be ruled out. Criteria for children 15 months to 12 years of age: - Patient must be HIV antibody-positive by repeated reactive screening test (e.g., ELISA) and positive confirmatory test (e.g., Western blot). OR - If antibody-negative, patient must have two positive p24 antigen determinations performed at least one week apart or have had a positive HIV culture. Patients must meet one of the following criteria: - Have at least one of the class P-2 symptoms (by CDC criteria). - Be immunosuppressed defined as having CD4+(T4) lymphocytes = or < 400 cells/mm3, based on two measurements at least 1 week apart. Exclusion Criteria Co-existing Condition: Patients with known hypersensitivity to AZT are excluded. Patients with the following are excluded: - Failure to meet inclusion criteria. - Inability to obtain signed informed consent from a parent or legal guardian. - Enrollment in another treatment protocol that expressly prohibits concomitant treatment with zidovudine (AZT). - Enrollment in another clinical trial in which AZT is a treatment. - Known hypersensitivity to AZT.
linkedct:description Previous studies with pediatric patients have shown improvements in clinical, immunologic, and virologic parameters with administration of AZT. This Treatment IND (investigational new drug) is an open label, uncontrolled protocol. AZT is ordered and prescribed by the patient's physician. The physician is responsible for obtaining informed consent, assuring that the patient meets the eligibility criteria, dispensing the medication to the patient, monitoring the patient's condition on treatment, and reporting required data to the project coordinating center.
linkedct:download_date Information obtained from ClinicalTrials.gov on December 30, 2009
linkedct:eligibility_gender Both
linkedct:eligibility_healthy_volunteers No
linkedct:eligibility_maximum_age 12 Years
linkedct:eligibility_minimum_age 3 Months
linkedct:enrollment 0 (xsd:int)
linkedct:firstreceived_date November 2, 1999
linkedct:id NCT00000662
rdfs:label Trial NCT00000662
linkedct:lastchanged_date August 1, 2008
linkedct:lead_sponsor_agency National Institute of Allergy and Infectious Diseases (NIAID)
linkedct:location <http://static.linkedct.org/resource/location/167038>
linkedct:nct_id NCT00000662
linkedct:number_of_arms 0 (xsd:int)
linkedct:number_of_groups 0 (xsd:int)
linkedct:official_title A Treatment IND for Retrovir Brand Zidovudine (AZT) Therapy of Pediatric Patients With HIV Disease
linkedct:org_study_id TX 304
linkedct:overall_status Active, not recruiting
linkedct:oversight <http://static.linkedct.org/resource/oversight/2918>
foaf:page <http://clinicaltrials.gov/show/NCT00000662>
linkedct:phase N/A
linkedct:secondary_id FDA 43A
linkedct:source National Institute of Allergy and Infectious Diseases (NIAID)
linkedct:study_design Treatment
linkedct:study_type Interventional
linkedct:summary To facilitate the use of zidovudine (AZT) in children who are 3 months to 12 years of age who are HIV-infected and either symptomatic or have a CD4 cell count < 400 cells/mm3 and to monitor adverse effects of AZT. Previous studies with pediatric patients have shown improvements in clinical, immunologic, and virologic parameters with administration of AZT.
rdf:type linkedct:trials
linkedct:verification_date April 1992