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NCT00000684 · ClinicalTrials.gov registry record · NA

Continuous High-Dose Intravenous Dextran Sulfate in Human Immunodeficiency Virus-Infected Individuals

A NA study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

Completed
Registry status
NA
Development phase
10
Enrollment target

NCT00000684: Completed NA study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

NCT00000684 is a NA study that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 10 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00000684, a NA study, has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

COMPLETED
Registry status
NA
Development phase
10 participants
Enrollment target

Study Summary

To determine the safety and effectiveness of dextran sulfate when it is administered intravenously at the maximum tolerated dose (MTD) as a treatment for HIV infection in AIDS patients. The effect of dextran sulfate on platelet survival will also be assessed in 3 patients to help determine the mechanism of thrombocytopenia (low platelets) noted in all patients receiving intravenous dextran sulfate in this study. Dextran sulfate appears to inhibit HIV in experiments in the test tube, but studies conducted in humans to determine its effect on HIV when dextran sulfate is given orally have not been conclusive. It is hoped that this study will show that dextran sulfate administered intravenously

Interventions

  • DRUG Dextran sulfate

Trial Details

FieldValue
Enrollment Target 10 participants
Est. Completion 1991-04
Phase NA

What the finished NCT00000684 record still lists

NCT00000684 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which Dextran sulfate is the first listed.

NCT00000684 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00000684 about?

NCT00000684 is a clinical study titled "Continuous High-Dose Intravenous Dextran Sulfate in Human Immunodeficiency Virus-Infected Individuals". To determine the safety and effectiveness of dextran sulfate when it is administered intravenously at the maximum tolerated dose (MTD) as a treatment for HIV infection in AIDS patients. The effect of dextran sulfate on platelet survival will also be assessed in 3 patients to help determine the mecha...

What is the current status of trial NCT00000684?

This trial is currently completed. It is a NA study. The enrollment target is 10 participants. Estimated completion is 1991-04.

What interventions are being tested in trial NCT00000684?

The interventions under investigation include: Dextran sulfate (DRUG).

Who is sponsoring clinical trial NCT00000684?

This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00000684's enrollment target sits among peer trials

10 1927th of 2000 higher than 26 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00000684, the US trial registry maintained by the National Library of Medicine. NCT00000684 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.