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NCT06955715Recruiting

Pasteurized Donor Human Milk for HIV-Exposed Infants: A Pilot Study

Source: ClinicalTrials.gov · Last updated 19 Nov 2025

Brief summary (registry, in English)

Pasteurized Donor Human Milk (PDHM) is recognized as providing vital immunological and nutritional benefits to vulnerable infants. Although PDHM is widely used in neonatal intensive care units (NICUs) to prevent infections (necrotizing enterocolitis) and improve infant health outcomes, its use for other populations, such as HIV-exposed infants, has been minimal. Pasteurized donor human milk is included in the 2023 Canadian Paediatric Society clinical consensus as a potential way to provide HIV-exposed infants some of the immunological benefits of human milk in a safe manner, as opposed to exclusive formula feeding (which is currently considered the gold standard for HIV-exposed infants). These new consensus guidelines also include recommendations to support those who wish to breastfeed using a harm reduction approach (e.g., increased viral load monitoring by peds infectious diseases), given the low risk of transmission in those adhering to antiretroviral medications. However, mixed feeding (e.g., breastfeeding and provision of infant formula) is not recommended, due to the potential for micro abrasions in the gastrointestinal epithelium as a result of the protein size in infant formula (which is larger and more abrasive than in human milk), which may increase the risk of HIV transmission if the HIV virus is present in breastmilk. As such, donor milk also presents a possible solution to support those who choose to breastfeed, but who may require a temporary supplement for whatever reason (e.g., nipple cracks, mastitis, etc.), as donor milk is human milk, thus has the same size of proteins and does not pose the same risk as infant formula in damaging the epithelial layer in the gut. Overall, major obstacles remain that prevent newborns outside of the NICU from regularly having access to donor human milk. These obstacles are illustrated by the high cost of donor milk, which is not covered by government programs, and the lack of information about the clinical benefits (for both those who choose to breastfeed or formula feed), acceptability of caregivers for this feeding option, and feasibility of providing donor human milk outside of a hospital setting. The investigators aim to determine whether giving PDHM to infants exposed to HIV is a practical possibility and learn from caregivers about any challenges associated with this feeding option. The results of this study will guide future research and a potential provincial initiative to expand access to PDHM for this population.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
10 (estimated)
First submitted
15 Apr 2025
Start date
15 Apr 2025
Primary completion date
1 May 2026
Lead sponsor
University of Saskatchewan
Diseases
HIV
NCT number
NCT06955715

What you commit to

  • Study type: Interventional
  • Planned participants: 10
  • From 15 Apr 2025 to the primary completion date, 1 May 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Who the study is looking for

  • ≥15 years of age
  • Pregnant or recently gave birth and living with HIV or is the primary caregivers of an HIV-exposed infant
  • Being followed by SHA Pediatric Infectious Disease
  • Saskatchewan resident (living within \~150 km from the University of Saskatchewan)
  • Have a household freezer
  • Willing to participate

Age in the registry: 15 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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SiteCityCountrySite status
University of Saskatchewan
Coordinator of this site? Confirm its status
SaskatoonCanadaRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.