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CompletedNCT00000657Updated Nov 3, 2021

Comparison of 2',3'-Dideoxyinosine (Didanosine, ddI) and Zidovudine in Therapy of Patients With the AIDS Dementia Complex

A Phase 2 interventional study of Zidovudine and Didanosine in AIDS Dementia Complex and HIV Infections, sponsored by National Institute of Allergy and Infectious Diseases (NIAID). Completed at 13 sites in United States. Open to participants aged 12 Years and older. Per ClinicalTrials.gov, last updated 2021-11-03.

Sponsored by National Institute of Allergy and Infectious Diseases (NIAID) · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
80
Ages
12 Years and older
Sex
All
01

Study summary

To compare the safety and effectiveness of orally administered didanosine (ddI) with high dose orally administered zidovudine (AZT) in patients who develop or exhibit progression of the AIDS dementia complex (ADC) and who have not previously been intolerant to AZT at doses of up to 1000 mg/day.

HIV-infected or AIDS patients may develop ADC which causes damage to the nervous system. ADC may be caused by some action of the AIDS virus on the nervous system, although similar problems can be caused by other infections because the AIDS virus lowers the body's ability to fight other infections. It is important to determine whether symptoms are due to ADC or to some other infection since treatment varies for different conditions. AZT has been shown to be beneficial to people with ADC although its effectiveness has only been studied in a small number of patients. Studies suggest that higher doses of AZT are more likely to be effective than standard doses in improving symptoms of ADC.

Read the detailed description

HIV-infected or AIDS patients may develop ADC which causes damage to the nervous system. ADC may be caused by some action of the AIDS virus on the nervous system, although similar problems can be caused by other infections because the AIDS virus lowers the body's ability to fight other infections. It is important to determine whether symptoms are due to ADC or to some other infection since treatment varies for different conditions. AZT has been shown to be beneficial to people with ADC although its effectiveness has only been studied in a small number of patients. Studies suggest that higher doses of AZT are more likely to be effective than standard doses in improving symptoms of ADC.

Patients are randomly assigned to receive either oral ddI or oral AZT.

02

Conditions studied

  • AIDS Dementia Complex
  • HIV Infections

Keywords

  • Didanosine
  • Drug Evaluation
  • Drugs, Investigational
  • AIDS Dementia Complex
  • Zidovudine
03

Who can participate

Ages eligible
12 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Concurrent Medication:

Allowed:

  • Chronic suppressive therapy for herpes simplex virus, cytomegalovirus, Candida albicans, and Salmonella.
  • Prophylactic therapy for Pneumocystis carinii pneumonia.
  • Maintenance anticonvulsant therapy following a seizure in the context of the AIDS dementia complex.
  • Isoniazid only if no acceptable alternative therapy is available.
  • Judicious use of benzodiazepines, tricyclics, and other antidepressants is allowed but a stable dose level should be obtained prior to entry and maintained throughout the trial.
  • In patients for whom it is medically necessary to initiate or alter therapy with these drugs during the initial 16 week study period, data will not be used in the study.
  • Metronidazole for single courses of therapy not to exceed 14 days within consecutive 90-day intervals, the first of which begins at the initiation of the study.
  • Erythropoietin for patients under the relevant Treatment IND.
  • Symptomatic therapies (such as analgesics, antihistamines, antiemetics, antidiarrheal agents).

Allowed but not encouraged:

  • trimethoprim /sulfamethoxazole (T/S) or other sulfonamides.

Patients must have the following:

  • Screened for other causes of dementia.
  • Stage 1, 2, or 3 AIDS dementia complex.
  • Estimated premorbid IQ of at least 70.
  • Anti-HIV antibody or HIV in blood and/or cerebrospinal fluid.
  • If prior history of positive syphilis serology, should have been treated with appropriate course of antibiotics; if not, such treatment should be administered prior to pretreatment screening.
  • Not have previously shown intolerance to zidovudine (AZT).
  • Able (or parent and/or guardian able) to provide written consent.

Allowed:

  • Basal cell carcinoma, in situ carcinoma of the cervix, Kaposi's sarcoma without evidence of visceral involvement or not requiring systemic chemotherapy.

Exclusion criteria

Exclusion Criteria

Co-existing Condition:

Patients with the following conditions or symptoms are excluded:

  • Grade 3 neuropathy, based on the Neuropathy Targeted Symptom.
  • Questionnaire, or patients with any moderate abnormality indicative of peripheral neuropathy including stocking loss of sensation (to sharp pain, light touch, or vibration), distal extremity weakness (\< 4/5), or absent ankle jerks.
  • History of present or past acute or chronic pancreatitis.
  • Active, symptomatic AIDS-defining opportunistic infection and requiring any ongoing maintenance therapy for confounding neurologic disease.
  • Severe premorbid psychiatric illness including bipolar illness, schizophrenia, and electroconvulsive therapy.

Previous neurological disease unrelated to HIV infection:

  • multiple sclerosis, documented stroke, degenerative disease.
  • Patients with chronic seizure disorders or head injury will only be excluded if the condition results in functional impairment or is likely to interfere with the evaluation.
  • Concurrent or previous central nervous system infections or neoplasms as revealed by Computerized Tomography (CT) or Magnetic Resonance Imaging (MRI) scan or cerebrospinal fluid analysis (such as toxoplasmosis, primary or metastatic Central Nervous System (CNS) lymphoma, progressive multifocal leukoencephalopathy, cryptococcal or other fungal meningitis, tuberculous Central Nervous System (CNS) infections, and untreated neurosyphilis).

Concurrent Medication:

Excluded:

  • Intravenous pentamidine. DHPG (Ganciclovir) should not be co-administered.
  • Monoamine oxidase (MAO) inhibitors, phenothiazines, butyrophenones, barbiturates, amphetamines.
  • Oral acidifying agents.

Patients with the following are excluded:

  • Neoplasms not specifically allowed.
  • Grade 3 neuropathy.
  • History of present or past acute or chronic pancreatitis.
  • Active, symptomatic AIDS-defining opportunistic infection.
  • Requiring any ongoing maintenance therapy for confounding neurologic disease.
  • Conditions listed under Exclusion Co-existing Conditions.

Prior Medication:

Excluded within 30 days of study entry:

  • Anti-HIV therapy other than zidovudine (AZT).
  • Biologic response modifiers.
  • Corticosteroids.
  • Drugs toxic to peripheral nerves.
  • Investigative drugs.
  • Neurotoxic drugs.

Excluded:

  • Dideoxycytidine (ddC).

Active alcohol or drug abuse or methadone maintenance sufficient, in the investigator's opinion, to prevent adequate compliance with study therapy and evaluations.

04

Study design

Phase
Phase 2
Primary purpose
Treatment
Masking
Double
Enrollment
80 participants

Interventions

  • DrugZidovudine
  • DrugDidanosine
05

Study locations

13 sites
  • San Francisco AIDS Clinic / San Francisco Gen Hosp
    San Francisco, California 941102859, United States
  • San Francisco Gen Hosp
    San Francisco, California 941102859, United States
  • Indiana Univ Hosp
    Indianapolis, Indiana 462025250, United States
  • Charity Hosp / Tulane Univ Med School
    New Orleans, Louisiana 70112, United States
  • Louisiana State Univ Med Ctr / Tulane Med School
    New Orleans, Louisiana 70112, United States
  • Tulane Univ School of Medicine
    New Orleans, Louisiana 70112, United States
  • Johns Hopkins Hosp
    Baltimore, Maryland 21287, United States
  • Univ of Minnesota
    Minneapolis, Minnesota 55455, United States
  • Mount Sinai Med Ctr
    New York, New York 10029, United States
  • Univ of Rochester Medical Center
    Rochester, New York 14642, United States
  • Univ of North Carolina
    Chapel Hill, North Carolina 275997215, United States
  • Julio Arroyo
    West Columbia, South Carolina 29169, United States
  • Univ of Washington
    Seattle, Washington 981224304, United States
06

References and documents

Publications

  • Brouwers P, Hendricks M, Lietzau JA, Pluda JM, Mitsuya H, Broder S, Yarchoan R. Effect of combination therapy with zidovudine and didanosine on neuropsychological functioning in patients with symptomatic HIV disease: a comparison of simultaneous and alternating regimens. AIDS. 1997 Jan;11(1):59-66. doi: 10.1097/00002030-199701000-00009. PubMed 9110076 ↗
07

Registry details

Key details

Study ID
NCT00000657
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborators
Bristol-Myers Squibb, Glaxo Wellcome
Responsible party
Sponsor
First posted
Aug 31, 2001
Completion
Sep 1992
Last update
Nov 3, 2021

Study contacts

C Hall
study chair
View the source record on ClinicalTrials.gov ↗

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