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NUSTART

Nutritional support for African adults starting antiretroviral therapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR201106000300631
Enrollment
2300
Registered
2011-05-31
Start date
2011-06-06
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV/AIDS

Interventions

Micronutrient and mineral supplement
Placebo

Sponsors

London School of Hygiene & Tropical Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: at least 18 years old; ART-naive (except for standard regimens to prevent maternal-to-child HIV transmission); BMI < 18.5 kg/m2. In the presence of clinical oedema and a BMI < 20 kg/m2, BMI will be re-measured after loss of oedema, and the patient considered eligible if BMI < 18.5 kg/m2 and ART has not yet been initiated; requiring ART as determined by CD4 count < 350/ul or stage 3 or 4 disease; willing to undertake intensive ART follow-up in the study clinic; providing written, fully informed consent (thumbprint will be accepted)

Exclusion criteria

Exclusion criteria: participation in a potentially conflicting research protocol; pregnancy (by self-report)

Design outcomes

Primary

MeasureTime frame
Mortality

Secondary

MeasureTime frame
Hospitalisation;Any SAE;Weight gain;Appetite;Grip strength;Change in fat-free mass and fat mass ;Plasma electrolytes;Iron status

Countries

Tanzania, Zambia

Contacts

Public ContactYolanda Fernandez

Project Administrator

Yolanda.Fernandez@lshtm.ac.uk+44 20 7958 8108

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026