search
Back to results

Impact of Cotrimoxazole Prophylaxis for HIV-Infected Adults on Antifolate Resistance

Primary Purpose

HIV, Malaria, Diarrhea

Status
Completed
Phase
Phase 4
Locations
Kenya
Study Type
Interventional
Intervention
Cotrimoxazole (trimethoprim sulfamethoxazole)
Sponsored by
Centers for Disease Control and Prevention
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional educational/counseling/training trial for HIV focused on measuring HIV, malaria, E. Coli, S. pneumoniae, drug resistance, antifolate, opportunistic infections, Africa, Kenya, East Africa

Eligibility Criteria

15 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Clients presenting to the CRC HIV counseling and testing site in Kisumu were eligible for the study if they met the following inclusion criteria: 15 years of age or older Able to make all follow-up visits (i.e. do not plan to leave Kisumu during the next 6 months, are not homebound) Able to understand and give informed consent. Exclusion Criteria: Clients were not eligible for the study if they met any of the following exclusion criteria: Known allergic reaction to sulfa medications (i.e. CTX, sulfadoxine- pyrimethamine) Women in their first trimester of pregnancy or planning to become pregnant in the next 6 months Clients taking daily antibiotics for treatment of a chronic illness; or prophylaxis, excluding tuberculosis treatment.

Sites / Locations

  • CDC KEMRI Research Institute

Outcomes

Primary Outcome Measures

Change in Plasmodium falciparum molecular markers of antifolate resistance before and while taking daily CTX
Change in nasopharyngeal pneumococcal resistance before and while taking daily CTX, and among children living in households where adults are taking daily CTX
Change in commensal E. coli resistance before and while taking daily CTX

Secondary Outcome Measures

To measure CTX-resistance among Salmonella and other enteric bacterial pathogens in patients with diarrhea in the study area
To assess the efficacy of sulfadoxine-pyrimethamine (SP) treatment of breakthrough P. falciparum parasitemia and clinical malaria among HIV-infected persons taking daily CTX prophylaxis
To measure sulfa metabolite levels in HIV-infected persons receiving daily CTX who develop a drug reaction, to determine if differing rates of metabolism contribute to the development of adverse reactions
To assess the effect of daily CTX prophylaxis on the etiology of diarrheal diseases in HIV-infected persons
To evaluate the serotype distribution of and immune response to colonizing pneumococci
To assess the cause of diarrheal diseases among HIV-infected persons
To measure the change in quality of life indicators among clients receiving daily CTX

Full Information

First Posted
August 29, 2005
Last Updated
December 12, 2005
Sponsor
Centers for Disease Control and Prevention
Collaborators
Kenya Medical Research Institute
search

1. Study Identification

Unique Protocol Identification Number
NCT00137657
Brief Title
Impact of Cotrimoxazole Prophylaxis for HIV-Infected Adults on Antifolate Resistance
Official Title
An Evaluation of the Impact of Cotrimoxazole Prophylaxis for HIV-Infected Adults on the Development of Antifolate Resistance Among Plasmodium Falciparum, Streptococcus Pneumoniae, and Escherichia Coli
Study Type
Interventional

2. Study Status

Record Verification Date
August 2005
Overall Recruitment Status
Completed
Study Start Date
February 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
November 2003 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Centers for Disease Control and Prevention
Collaborators
Kenya Medical Research Institute

4. Oversight

5. Study Description

Brief Summary
At least three studies in sub-Saharan Africa have demonstrated a decrease in morbidity or mortality among HIV-infected adults who took daily cotrimoxazole (trimethoprim sulfamethoxazole) [CTX] prophylaxis. Because of the demonstrated beneficial effect, high tolerability and low cost of CTX, the United Nations Programme on HIV/AIDS (UNAIDS) recommends that HIV-infected persons with symptomatic HIV or depressed CD4 counts receive daily CTX. The effect of this recommendation on subsequent development of antimicrobial resistance to antifolates among important pathogens needs to be evaluated. The investigators measured the change in the prevalence of markers of antifolate resistance among P. falciparum, and the change in the prevalence of CTX resistance among S. pneumoniae, and E. coli in HIV-infected individuals receiving CTX daily prophylaxis. In addition, the investigators measured the change in the prevalence of naso-pharyngeal or oro-pharyngeal carriage of CTX resistant S. pneumoniae among children living in households where an HIV-infected adult was receiving CTX daily prophylaxis.
Detailed Description
We conducted this study in Kisumu, Kenya where HIV prevalence is high and malaria is highly endemic. HIV infected and uninfected adults were assigned to receive daily CTX if CD4 cell count was <350, or daily multivitamin if CD4 cell count was >= 350 or if the client was HIV negative. All clients were then followed for a total of 6 months. At specified scheduled and sick visits, clients received a physical exam, blood smears, nasopharyngeal swabs and stool samples or rectal swabs. Samples collected at baseline and during follow-up were used to measure the change in CTX resistance among P. falciparum parasites, pneumococcus isolates, and commensal E. coli.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV, Malaria, Diarrhea, Pneumonia, Opportunistic Infections
Keywords
HIV, malaria, E. Coli, S. pneumoniae, drug resistance, antifolate, opportunistic infections, Africa, Kenya, East Africa

7. Study Design

Primary Purpose
Educational/Counseling/Training
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
1478 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Cotrimoxazole (trimethoprim sulfamethoxazole)
Primary Outcome Measure Information:
Title
Change in Plasmodium falciparum molecular markers of antifolate resistance before and while taking daily CTX
Title
Change in nasopharyngeal pneumococcal resistance before and while taking daily CTX, and among children living in households where adults are taking daily CTX
Title
Change in commensal E. coli resistance before and while taking daily CTX
Secondary Outcome Measure Information:
Title
To measure CTX-resistance among Salmonella and other enteric bacterial pathogens in patients with diarrhea in the study area
Title
To assess the efficacy of sulfadoxine-pyrimethamine (SP) treatment of breakthrough P. falciparum parasitemia and clinical malaria among HIV-infected persons taking daily CTX prophylaxis
Title
To measure sulfa metabolite levels in HIV-infected persons receiving daily CTX who develop a drug reaction, to determine if differing rates of metabolism contribute to the development of adverse reactions
Title
To assess the effect of daily CTX prophylaxis on the etiology of diarrheal diseases in HIV-infected persons
Title
To evaluate the serotype distribution of and immune response to colonizing pneumococci
Title
To assess the cause of diarrheal diseases among HIV-infected persons
Title
To measure the change in quality of life indicators among clients receiving daily CTX

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clients presenting to the CRC HIV counseling and testing site in Kisumu were eligible for the study if they met the following inclusion criteria: 15 years of age or older Able to make all follow-up visits (i.e. do not plan to leave Kisumu during the next 6 months, are not homebound) Able to understand and give informed consent. Exclusion Criteria: Clients were not eligible for the study if they met any of the following exclusion criteria: Known allergic reaction to sulfa medications (i.e. CTX, sulfadoxine- pyrimethamine) Women in their first trimester of pregnancy or planning to become pregnant in the next 6 months Clients taking daily antibiotics for treatment of a chronic illness; or prophylaxis, excluding tuberculosis treatment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mary J Hamel, M.D.
Organizational Affiliation
Centers for Disease Control and Prevention
Official's Role
Principal Investigator
Facility Information:
Facility Name
CDC KEMRI Research Institute
City
Kisumu
Country
Kenya

12. IPD Sharing Statement

Learn more about this trial

Impact of Cotrimoxazole Prophylaxis for HIV-Infected Adults on Antifolate Resistance

We'll reach out to this number within 24 hrs