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Comparison · NCT04692467-bb8ddf6e

Intervention (Early Hypertension) vs Standard of Care: Number of Participants Who Are Enrolled at Baseline and Remain in the Study by 12 Months

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Intervention (Early Hypertension) vs Standard of Care: Number of Participants Who Are Enrolled at Baseline and Remain in the Study by 12 Months. Trial comparisons, record NCT04692467-bb8ddf6e. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04692467-bb8ddf6e

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.9840.9430.996wilson
Risk in group 20.9680.920.987wilson
Risk difference, group 1 minus group 20.0161-0.02910.0653newcombe hybrid score
Risk ratio, group 1 over group 21.020.9781.06log
Odds ratio, group 1 over group 22.030.36611.3log
Number needed to treat, for one more participant with the outcome on Intervention (Early Hypertension) than on Standard of Care62from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: standard of care.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Intervention (Early Hypertension)
Participants randomized to the early HTN treatment arm will initiate 5mg daily of amlodipine immediately, increasing to 10 mg if SBP \>130 mmHg after 1 month.~Amlodipine 5mg: Amlodipine, Haiti's first-line antihypertensive medication, will be administered to the intervention group.
122124OG000
Group 2Standard of CareParticipants randomized to the SOC arm will not be initiated on any medications initially. They may be initiated on amlodipine only if they develop HTN (SBP ≥140 or DBP ≥90 mm Hg).120124OG001

Outcome

Type
SECONDARY
Title
Number of Participants Who Are Enrolled at Baseline and Remain in the Study by 12 Months
Description
All participants were included in enrolment. Remaining in the study was defined as having a clinic visit at month 12 (final study visit).
Time frame
Baseline, 12 months
Population
2 participants in the standard of care arm were excluded from analysis because these participants died of causes unrelated to the research prior to follow-up month 12.

Source ClinicalTrials.gov

Trial

Title
Treatment of Early Hypertension Among Persons Living With HIV in Haiti
NCT number
NCT04692467
Phases
PHASE2
Conditions
HIV/AIDS, Pre Hypertension
Interventions
Amlodipine 5mg
Lead sponsor
Weill Medical College of Cornell University
Results first posted
2024-04-09

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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