HIV/AIDS Clinical Trial
— E4EOfficial title:
Does Provision of Point of Care CD4 Technology and Early Knowledge of CD4 Levels Affect Early Initiation and Retention on Anti-retroviral Treatment (ART) in HIV Positive Pregnant Women in the Context of Option B+ for PMTCT?
The study will be conducted at 32 health care facilities in three provinces in Zimbabwe and
will compare the impact of the provision Point of Care CD4 technology and early knowledge of
CD4 levels on retention at 12 months, with or without POC CD4 and a programmatic mentoring
package. Option B+ will be implemented at all sites and 16 intervention sites will receive
POC CD4 machines and visits from a team of clinical mentors.
The study also aims to assess rates of ART initiation and time to ART initiation of HIV
positive pregnant women in settings implementing option B+ with or without POC CD4 and
related counselling/support; rates of retention in care of HIV positive mothers at 6 months
post ART initiation in settings implementing option B+ with or without POC CD4 and related
counselling/support; rates of ART initiation and retention at 6 and 12 months post ART
initiation according to different levels of CD4 count; cost of retaining HIV positive
pregnant women until 6 and 12 months; acceptability and feasibility of POC CD4 as an adjunct
to good clinical care of HIV positive pregnant women.
Status | Recruiting |
Enrollment | 704 |
Est. completion date | July 2016 |
Est. primary completion date | June 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Pregnant at the time of booking - HIV positive diagnosis - Not on ART at the time of booking - Present up to 38 weeks into gestation - Presents more than 48 hours prior to delivery Exclusion Criteria: - Already on ART at booking - Presents more than 38 weeks into gestation or less than 48 hours prior to delivery |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Zimbabwe | Chamnangana | Beitbridge | Matebeleland South |
Zimbabwe | Zezani | Beitbridge | Matebeleland South |
Zimbabwe | Mdutshane RHC | Bubi | Matebeleland North |
Zimbabwe | Membeswana RHC | Bubi | Matebeleland North |
Zimbabwe | Huwana RHC | Bulilima | Matebeleland South |
Zimbabwe | Madlambudzi | Bulilima | Matebeleland South |
Zimbabwe | Bromley | Goromonzi | Mashonaland East |
Zimbabwe | Henry John Rheimer | Goromonzi | Mashonaland East |
Zimbabwe | Kubatsirana | Goromonzi | Mashonaland East |
Zimbabwe | Melfort | Goromonzi | Mashonaland East |
Zimbabwe | Mwanza RHC | Goromonzi | Mashonaland East |
Zimbabwe | Mzimuni | Gwanda | Matebeleland South |
Zimbabwe | West Nicholson Zimcare | Gwanda | Matebeleland South |
Zimbabwe | Sanale RHC | Insiza | Matebeleland South |
Zimbabwe | Zhulube | Insiza | Matebeleland South |
Zimbabwe | Lupaka | Lupane | Matebeleland North |
Zimbabwe | Dingimuzi | Mangwe | Matebeleland South |
Zimbabwe | Border Church RHC | Marondera | Mashonaland East |
Zimbabwe | Chipararwe | Marondera | Mashonaland East |
Zimbabwe | Lustleigh | Marondera | Mashonaland East |
Zimbabwe | Masikana | Marondera | Mashonaland East |
Zimbabwe | Kezi | Matobo | Matebeleland South |
Zimbabwe | Matopo Hospital | Matobo | Matebeleland South |
Zimbabwe | Charehwa | Mutoko | Mashonaland East |
Zimbabwe | Kushinga RHC | Mutoko | Mashonaland East |
Zimbabwe | Nyamazuwe Rural Hospital | Mutoko | Mashonaland East |
Zimbabwe | Masasa | Seke | Mashonaland East |
Zimbabwe | Madlangombe | Tsholotsho | Matebeleland North |
Zimbabwe | Makhaza RHC | Tsholotsho | Matebeleland North |
Zimbabwe | Mbembesi | Umguza | Matebeleland North |
Zimbabwe | Mashambanhaka | UMP | Mashonaland East |
Zimbabwe | Hlangano | Umzingwane | Matebeleland South |
Lead Sponsor | Collaborator |
---|---|
WHO, Department of Maternal, Newborn, Child and Adolescent Health | Canadian International Development Agency, Netherlands: Ministry of Health, Welfare and Sports |
Zimbabwe,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Retention | Proportion of HIV positive pregnant women that are retained on ART, 12 months after initiation | 12 months | No |
Secondary | Time-to-initiation | Median time-to-initiation between HIV positive diagnosis and enrolment onto Option B+ with or without POC CD4 and related counseling/support | 12 months | No |
Secondary | Retention at 6 months | Proportion of HIV positive pregnant women that are retained on ART, 6 months after initiation in settings implementing option B+ with or without POC CD4 and related counseling/support | 6 months | No |
Secondary | Retention by CD4 count | Proportion of women initiated and retained on ART at 6 and 12 months post ART initiation, according to different levels of CD4 count | 6 months , 12 months | No |
Secondary | Cost per pregnant woman retained on ART | 6 months , 12 months | No | |
Secondary | Initiation within 1 month | Proportion of HIV positive pregnant women initiating ART within 1 month of positive HIV test | 1 month | No |
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