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Completed

NCT Number: NCT03642704

HIV Diagnosis and Treatment at Birth for Newborn With High Risk HIV Exposure

Principal objective Assess the operational efficacy of a strategy combining early diagnosis and preventive antiretroviral treatment systematically reinforced from the birth* among infants at high risk of infection with HIV** .

* in a maximum of 48 hours after delivery

* born from HIV infected mothers who received less than 4 weeks of antiretroviral therapy prior delivery and / or HIV infection diagnosed at delivery

Intervention, a combined strategy :

After positive HIV infection screening from mother in the delivery room and put on antiretroviral treatment of mothers with post partum according to national guidelines , newborns benefit :

* Early detection of HIV infection at birth * Without awaiting the outcome of early detection result, a preventive reinforced antiretroviral treatment (zidovudine, lamivudine, nevirapine or zidovudine, lamivudine if their mother is infected with HIV-2), from birth for 12 weeks. * Regular HIV screening until the end of breastfeeding or later to 18 months. * In case of positive results of an HIV test, an antiretroviral treatment with zidovudine, lamivudine, lopinavir, ritonavir whatever serology HIV 1 or 2.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Hôpital National Ignace Deen

Conakry, Guinea

About this study

Objectives Principal objective Assess the operational efficacy of a strategy combining early diagnosis and preventive antiretroviral treatment systematically reinforced from the birth* among infants at high risk of infection with HIV** .

  • in a maximum of 48 hours after delivery

**born from HIV infected mothers who received less than 4 weeks of antiretroviral therapy prior delivery and / or HIV infection diagnosed at delivery Secondary objectives

  • Measure the cascade management of HIV infected mothers and HIV infected infants
  • Measure the tolerance of reinforced preventive antiretroviral treatment
  • Describe the rate of mother to child transmission of HIV and its risk factors
  • Describe the clinical and immuno-virologic outcomes in mothers, in HIV infected children and in HIV-non-infected children
  • Evaluate the acceptability of the strategy by mothers and caregivers.
  • Compare the early diagnosis of HIV infection with Abbott and Biocentric HIV RNA tests

Methodology Prospective non-comparative study of mother-child pairs whose mother is HIV-infected and received less than 4 weeks of antiretroviral therapy before birth or whose HIV infection has been diagnosed at birth.

Estimated enrolment: 300 mother-child pairs

Eligibility:

Inclusion criteria

Mother-child pairs whose mother is HIV-infected and received less than 4 weeks of antiretroviral therapy before delivery or whose HIV infection has been diagnosed at delivery Mother who signed the informed consent form to participate in the study.

non-inclusion criteria: Mother treated with antiretrovirals during the month preceding delivery No inclusion for precautionary reason : clinical symptoms suggesting an opportunistic infection of the central nervous system.

No inclusion for monitoring difficulties History or presence of allergy to the study drugs or their components Contra-indications to the study drugs Symptoms, physical signs or laboratory values suggestive of systemic disorders, (including renal, hepatic, cardiovascular, pulmonary, skin, or psychiatric and other conditions, which could interfere with the interpretation of the trial results

Intervention, a combined strategy :

After positive HIV infection screening from mother in the delivery room and put on antiretroviral treatment of mothers with post partum according to national guidelines , newborns benefit :

  • Early detection of HIV infection at birth
  • Without awaiting the outcome of early detection result, a preventive reinforced antiretroviral treatment (AZT / 3TC / NVP or AZT / 3TC if their mother is infected with HIV -2), from birth for 12 weeks.
  • Regular HIV screening until the end of breastfeeding or later to 18 months.
  • In case of positive results of an HIV test, an antiretroviral treatment with AZT / 3TC / LPV whatever serology HIV 1 or 2.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Mother-child pairs whose mother is HIV-infected and received less than 4 weeks of antiretroviral therapy before delivery or whose HIV infection has been diagnosed at delivery
  • Mother who signed the informed consent form to participate in the study.

Exclusion criteria

  • Mother treated with antiretrovirals during the month preceding delivery
  • No inclusion for precautionary reason : clinical symptoms suggesting an opportunistic infection of the central nervous system.
  • No inclusion for monitoring difficulties
  • History or presence of allergy to the study drugs or their components
  • Symptoms, physical signs or laboratory values suggestive of systemic disorders, (including renal, hepatic, cardiovascular, pulmonary, skin, or psychiatric and other conditions, which could interfere with the interpretation of the trial results

Treatment and study plan

Reinforced preventive ARV therapy

Drug

If the mother is HIV-1 or HIV 1/2 infected:

  • zidovudine / laminvudine (60/30 mg), ¼ cp morning and evening orally for 12 weeks.
  • nevirapine: 15mg/OD if weight ≥ 2500g / 10mg/OD if weight = 2000-2499g / 2mg/kg/OD if weight < 2000g for 12 weeks in case of HIV-1 infection. After 6 weeks, nevirapine will increase at 20mg/OD

If the mother is HIV-2 infected:

  • zidovudine / laminvudine (60/30 mg), ¼ cp morning and evening orally for 12 weeks.

Other names: Early diagnosis in children exposed to HIV

Primary outcomes

  1. Proportion of newborns who have received an HIV diagnosis and reinforced preventive antiretroviral treatment at birth.

    Time frame: Day 2

    Proportion of newborns who have received both HIV test and reinforced preventive antiretroviral treatment in a maximum of 48 hours after birth.

Secondary outcomes

  1. Proportion of mothers diagnosed with HIV who will initiate an antiretroviral therapy

    Time frame: Week 72

    • Proportion of mothers diagnosed with HIV at Day 0 who will initiate an antiretroviral therapy
  2. Proportion of children diagnosed with HIV who will initiate an antiretroviral therapy

    Time frame: Week 72

    • Proportion of children diagnosed with HIV from Day 0 to Week 72 who will initiate an antiretroviral therapy
  3. Proportion of mother-child pairs retained in the study with child having 2 PCR performed after stopping reinforced preventive antiretroviral treatment

    Time frame: Week 24

    • Proportion of mother-child pairs retained in the study from Day 0 to Week 24 with child having 2 PCR performed after stopping reinforced preventive antiretroviral treatment
  4. Proportion of mother-child pairs retained in the study

    Time frame: Week 72

    • Proportion of mother-child pairs retained in the study from Day 0 to Week 72.

Other outcomes

  1. Measure the clinical tolerance of reinforced preventive antiretroviral treatment in children

    Time frame: Week 12

    • Nature of clinical adverse events
  2. Measure the biological tolerance of reinforced preventive antiretroviral treatment in children

    Time frame: Week 12

    • Nature of biological adverse events
  3. Measure the proportion of children on reinforced preventive antiretroviral treatment with anemia

    Time frame: Week 12

    • Proportion of children with anemia superior or equal to grade 2
  4. Measure the proportion of children who change antiretroviral therapy for grade 4 adverse event

    Time frame: Week 12

    • Proportion of children who change antiretroviral therapy for grade 4 adverse event
  5. Measure the proportion of children with preventive antiretroviral treatment interruption

    Time frame: Week 12

    • Proportion of children with preventive antiretroviral treatment interruption
  6. Describe the clinical events occurring in mothers

    Time frame: Week 72

    • Description of clinical events occurring in mothers
  7. Measure the proportion of mothers presenting clinical events

    Time frame: Week 72

    • Proportion of mothers presenting clinical events
  8. Describe the immunological outcomes in mothers

    Time frame: Week 72

    • Value of CD4 (absolute number)
  9. Describe the virological outcomes in mothers

    Time frame: Week 72

    • Value of HIV RNA (copies/mL)
  10. Describe the clinical outcomes in HIV-infected children

    Time frame: Week 48

    • Description of clinical events occurring in HIV-infected children
  11. Measure the proportion of HIV-infected children presenting clinical events

    Time frame: Week 48

    • Proportion of HIV-infected children presenting clinical events
  12. Describe the immunological outcomes in HIV infected children

    Time frame: Week 48

    • Value of CD4 (absolute number)
  13. Describe the virological outcomes in HIV infected children

    Time frame: Week 48

    • Value of HIV RNA (copies/mL)
  14. Describe the clinical outcomes in HIV-non-infected children

    Time frame: Week 72

    Nature of clinical events occurring in HIV-non-infected children

  15. Measure the proportion of HIV-non-infected children presenting clinical events

    Time frame: Week 72

    • Proportion of HIV-non-infected children presenting clinical events
  16. Describe the rate of mother to child transmission of HIV

    Time frame: Week 72

    • Proportion of HIV infected children (based on PCR ADN or ARN)
  17. Describe the risk factors of mother to child transmission of HIV

    Time frame: week 72

    Description of risk factors for HIV transmission

Sponsors and collaborators

Lead sponsor

ANRS, Emerging Infectious Diseases

Other Gov

Registry information

Official study title

HIV Diagnosis and Treatment at Birth for HIV Exposed Newborn Whose Mother Was Not Treated With Antiretroviral Therapy (ART) During Last Month Before Delivery : Strategy Evaluation in Guinea.

Acronym: DIAVINA

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Aug 22, 2018
Registry last updated
Oct 22, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.