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Inpatient Package to Reduce HIV and AIDS-related Death in Zambia

Inpatient Package to Reduce HIV and AIDS-related Death in Zambia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04033718
Acronym
IPADZ
Enrollment
72
Registered
2019-07-26
Start date
2021-10-01
Completion date
2024-06-30
Last updated
2024-08-09

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

Conditions

Cryptococcosis, HIV/AIDS, HIV Testing, Hospitalization, Transitions of Care, Tuberculosis

Brief summary

Early post-discharge mortality is high among HIV-infected Zambians admitted to the hospital. Likely this is in part due to missed opportunities to identify lethal coinfections and optimize HIV care during admission (and before discharge). In this study the investigators will develop and pilot a new approach to inpatient HIV care that follows international guidelines for management of advanced HIV disease.

Interventions

DIAGNOSTIC_TESTInpatient lab bundling

The investigators will provide patients a package of diagnostic tests at the time of admission to comprehensively assess for HIV coinfections and treatment failure. These labs are all recommended in advanced HIV guidelines but in this study we will provide all tests as a bundle rather than step-by-step as suggested in guidelines.

BEHAVIORALInpatient navigation

Participants will be assigned a patient navigator who will support the patient and bedsider (treatment supporter/guardian) during the hospitalization. The navigator will be an HIV counselor who can provide counseling and health education, as well as support specimen transport, obtaining results, booking tests in other departments, linkages to ART clinic, and discharge planning

Sponsors

University Teaching Hospital
CollaboratorUNKNOWN
University of Maryland
CollaboratorOTHER
University of Alabama at Birmingham
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 18+ years old * HIV-positive (by self-report or DCT result in UTH file) * Resident of Lusaka * Admitted to the hospital

Exclusion criteria

* Too sick to provide informed consent (based on clinician opinion) * Likely to be discharged in the next 48 hours (based on clinician opinion)

Design outcomes

Primary

MeasureTime frameDescription
Coinfection diagnosisThrough hospital discharge, an average of 2 weeksPositive test for tuberculosis or cryptococcus on admission

Countries

Zambia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026