Isoniazid Prophylaxis With Concomitant Cotrimoxazole in HIV-infected Children

• Sponsor: University of Cape Town (Other)
• Overall Status: Completed
• CT.gov ID: NCT00330304
• Collaborator: University of Stellenbosch (Other), Medical Research Council (Other), Rockefeller Foundation (Other)
• Enrollment: 450
• Locations: 2
• Arms: 2
• Actual Duration (Months): 106.4
• Patients Per Site: 225
• Patients Per Site Per Month: 2.1

Study Details

Study Description

Brief Summary

The study involves use of isoniazid and cotrimoxazole as strategies for preventing infections in HIV-infected children and reducing mortality. Cotrimoxazole is well known to reduce mortality and infections in HIV-infected children and is currently the recommended standard of care. However, isoniazid has only been studied in HIV-infected adults (in whom it has been shown to substantially reduce the incidence of tuberculosis). In a randomised controlled study of isoniazid in HIV-infected children, the investigators found that INH reduced mortality and tuberculosis incidence in excess of 50%; the data safety monitoring board recommended termination of the placebo arm given the beneficial effects of INH. The investigators therefore aim to follow-up these children to compare the long term impact of two different INH and CTX preventive regimens (daily versus thrice weekly) on morbidity, mortality, adherence and incidence of adverse reactions. The investigators also aim to investigate the efficacy, safety and tolerability of INH compared with placebo for prevention of TB in children receiving HAART as the benefit in this group is unknown.

Condition or Disease	Intervention/Treatment	Phase
Tuberculosis	Drug: Isoniazid; Drug: Cotrimoxazole; Drug: isoniazid; Other: placebo	Phase 3

Detailed Description

Tuberculosis (TB) and HIV are dual pandemics occurring in South Africa. Prevention of TB and the subsequent decline in immune function in HIV-infected children is an important strategy to reduce mortality. Isoniazid (INH) prophylaxis reduces TB incidence in HIV-infected adults, but the efficacy in HIV-infected children has not been studied. In 2003, the investigators therefore began a double blind placebo controlled trial to investigate the impact of INH prophylaxis on mortality, morbidity and TB incidence in HIV-infected children. Interim analysis found a striking reduction in mortality and TB with a decrease in mortality in excess of 50% and 60% respectively, in children on INH. Based on this, the placebo arm was terminated; the study continued as a trial of thrice versus daily INH and cotrimoxazole (CTX). Although the results indicate an important benefit in children on INH, it is unknown what the long term efficacy and safety of INH prophylaxis is, what the optimal regime is and whether this pertains to children on HAART (who formed a minority of the cohort but who are still at risk for TB).

Aim To investigate the efficacy, safety and tolerability of INH and CTX as prophylactic strategies for HIV-infected children in a high TB prevalence area.

Objectives

1. To compare the long term impact of two different INH preventive regimens (daily versus thrice weekly) on TB incidence, occurrence of INH resistance in patients with culture-confirmed TB, mortality, incidence of adverse reactions and adherence

2. To compare the long term impact of two different CTX prophylactic regimens (daily versus thrice weekly) on mortality, frequency and duration of hospitalization, type of serious infections, nasopharyngeal carriage of bacteria and development of antimicrobial resistance, adherence and incidence of adverse reactions

3. To investigate the efficacy, safety and tolerability of INH compared with placebo for prevention of TB in children receiving HAART

Methods A prospective randomized double blind placebo controlled study of INH versus placebo in newly recruited HIV-infected children who are stable on HAART. In addition, an extended follow-up study of children already randomised to thrice weekly or daily INH and CTX. Children will be followed for 2 years with regular clinical evaluation, adherence assessment and laboratory monitoring. Outcomes measured will be mortality, TB incidence, morbidity, adherence and tolerability.

Study Design

• Study Type: Interventional
• Actual Enrollment: 450 participants
• Allocation: Randomized
• Intervention Model: Factorial Assignment
• Masking: Double
• Primary Purpose: Prevention
• Official Title: Long Term Study of 2 Isoniazid (INH) Prophylactic Regimens With Concomitant Cotrimoxazole (CTX) in HIV-infected Children - Impact on Morbidity, Mortality, Bacterial Resistance and Incidence of Tuberculosis
• Actual Study Start Date: Jan 1, 2003
• Actual Primary Completion Date: Nov 15, 2011
• Actual Study Completion Date: Nov 15, 2011

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Isoniazid preventive therapy HIV infected children living in a high TB prevalence area receive isonaizid prophylaxis daily, together with cotrimoxazole prohpylaxis either 3 times a week or daily.	Drug: Isoniazid; isoniazid 10mg/kg orally, daily, for study period; Drug: Cotrimoxazole; Cotrimoxazole given 3 times a week or daily, orally, for study period; Drug: isoniazid; Isoniazid, 10mg/kg daily for study period
Placebo Comparator: Placebo HIV infected children living in a high TB prevalence area receive placebo once daily	Drug: Cotrimoxazole; Cotrimoxazole given 3 times a week or daily, orally, for study period; Other: placebo; Placebo tablet identicle in appearance to intervention: isoniazid table

Outcome Measures

Primary Outcome Measures

1. TB incidence [Jan 2003 to July 2011]

2. Mortality [Jan 2003 to July 2011]

Secondary Outcome Measures

1. intercurrent infections [Jan 2003 to July 2011]

2. adherence [Jan 2003 to July 2011]

3. adverse events [Jan 2003 to July 2011]

4. antimicrobial resistance [Jan 2003 to July 2011]

Eligibility Criteria

Criteria

• Ages Eligible for Study: 8 Weeks to 15 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• HIV-infected children

• Resident in Cape Town

• Informed consent obtainable

• weight > 2.5kg

• Access to transport

• HAART use for not less than 2 months but not more than 12 months with no significant demonstrated toxicity and good adherence

Exclusion Criteria:

• Chronic diarrhoea

• Current use of INH prophylaxis

• Prior hypersensitivity to INH prior history of allergy to sulphur drugs

• Prior history of allergy to sulphur drugs

• Severe anaemia (haemoglobin less than 7 gm/dl)

• Neutropenia (absoloute neutrophil count less than 400 cells)

• Thrombocytopenia (platelet count < 50 000/uL)

• Non-reversible renal failure

• Clinical hepatitis

• Exposure to household TB contact, requiring INH prophylaxis

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Red Cross Childrens Hospital	Cape Town	Western Cape	South Africa	7700
2	Tygerberg Hospital	Cape Town	Western Cape	South Africa

Sponsors and Collaborators

• University of Cape Town
• University of Stellenbosch
• Medical Research Council
• Rockefeller Foundation

Investigators

• Principal Investigator: Heather J Zar, MD PHd, University of Cape Town
• Principal Investigator: Mark Cotton, Md PhD, University of Stellenbosch

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Heather Zar, Professor, University of Cape Town
• ClinicalTrials.gov Identifier: NCT00330304
• Other Study ID Numbers: 299/2005
• First Posted: May 26, 2006
• Last Update Posted: Apr 22, 2019
• Last Verified: Apr 1, 2019

• Keywords provided by Heather Zar, Professor, University of Cape Town: Tuberculosis; Child; HIV; prophylaxis; mortality
• Additional relevant MeSH terms: Tuberculosis; Isoniazid; Trimethoprim, Sulfamethoxazole Drug Combination

Study Results

No Results Posted as of Apr 22, 2019