Completed

Phase 2
Age: 13Years +
All Genders
ID00000771

A Double-Blind, Placebo-Controlled Trial of Paromomycin for Treatment of Cryptosporidiosis in Patients With Advanced HIV Disease and CD4 Counts Under 150 Cells/mm3

Led by National Institute of Allergy and Infectious Diseases (NIAID) · Updated on 2021-11-04

68

Participants Needed

15

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

To determine the effectiveness of oral paromomycin sulfate for 21 days compared to placebo in the treatment of cryptosporidiosis in patients with HIV infection. To evaluate the safety of oral paromomycin at two different doses. To explore whether paromomycin administered over a longer period provides additional benefit. In previous studies, patients with cryptosporidiosis demonstrated dramatic improvement with paromomycin therapy.

CONDITIONS

Official Title

A Double-Blind, Placebo-Controlled Trial of Paromomycin for Treatment of Cryptosporidiosis in Patients With Advanced HIV Disease and CD4 Counts Under 150 Cells/mm3

Who Can Participate

Age: 13Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

Inclusion Criteria

Concurrent Medication:

Allowed:

  • Antiretroviral therapy.
  • Macrolides for disseminated Mycobacterium avium.
  • Atovaquone for toxoplasmosis.
  • Other antimicrobials for concurrent infections.
  • Lomotil, Imodium, or deodorized opium tincture in a standardized regimen for diarrhea.

Patients must have:

  • Advanced HIV disease.
  • Diarrhea presumptively caused by Cryptosporidia.

Exclusion Criteria

Co-existing Condition:

Patients with the following symptoms or conditions are excluded:

  • Hypersensitivity to aminoglycosides.
  • Inability to swallow capsules.
  • Active infection due to other enteric pathogens. Previous diagnosis of CMV or MAC infection permitted if patient is currently stabilized on a therapeutic regimen (clarithromycin up to 500 mg bid or azithromycin up to 600 mg daily).
  • Other known causes for diarrhea (e.g., malabsorption syndrome, gastrointestinal Kaposi's sarcoma).

Concurrent Medication:

Excluded during the first 9 weeks of study:

  • Agents with putative anticryptosporidial activity (such as spiramycin, diclazuril, letrazuril, or bovine colostrum).
  • Octreotide acetate (Sandostatin).
  • Antidiarrheals other than those specifically allowed.
  • Clarithromycin if initiated at 500 mg or higher or azithromycin if initiated at 600 mg or higher.

Prior Medication:

Excluded:

  • Paromomycin at > 1 g/day for >= 14 days prior to study entry.

Excluded within 14 days prior to study entry:

  • Agents with putative anticryptosporidial activity (such as spiramycin, diclazuril, letrazuril, or bovine colostrum), with the exception of macrolides that are permitted for other indications.
  • Octreotide acetate (Sandostatin).
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

Trial Site Locations

Total: 15 locations

1

USC CRS

Los Angeles, California, United States

Status Unknown

2

Univ. of Miami AIDS CRS

Miami, Florida, United States, 33136

Status Unknown

3

Northwestern University CRS

Chicago, Illinois, United States, 60611

Status Unknown

4

Rush Univ. Med. Ctr. ACTG CRS

Chicago, Illinois, United States, 60612

Status Unknown

5

Weiss Memorial Hosp.

Chicago, Illinois, United States, 60640

Status Unknown

6

Indiana Univ. School of Medicine, Infectious Disease Research Clinic

Indianapolis, Indiana, United States, 46202

Status Unknown

7

Methodist Hosp. of Indiana

Indianapolis, Indiana, United States, 46202

Status Unknown

8

Washington U CRS

St Louis, Missouri, United States

Status Unknown

9

SUNY - Buffalo, Erie County Medical Ctr.

Buffalo, New York, United States, 14215

Status Unknown

10

NY Univ. HIV/AIDS CRS

New York, New York, United States, 10016

Status Unknown

11

Cornell University A2201

New York, New York, United States, 10021

Status Unknown

12

Univ. of Cincinnati CRS

Cincinnati, Ohio, United States, 45267

Status Unknown

13

Case CRS

Cleveland, Ohio, United States, 44106

Status Unknown

14

The Ohio State Univ. AIDS CRS

Columbus, Ohio, United States, 43210

Status Unknown

15

Puerto Rico-AIDS CRS

San Juan, Puerto Rico

Status Unknown

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

N/A

Allocation

N/A

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

0

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Published Research Related To This Trial

Paromomycin: no more effective than placebo for treatment of cryptosporidiosis in patients with advanced human immunodeficiency virus infection. AIDS Clinical Trial Group.

R G Hewitt, C T Yiannoutsos, E S Higgs...

https://pubmed.ncbi.nlm.nih.gov/11049793