Comparison · NCT03070600-6eab54e2
Universal Arm- PrEP Initiated vs Targeted Arm- PrEP Initiated: PrEP Adherence by Self-report
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Universal Arm- PrEP Initiated vs Targeted Arm- PrEP Initiated: PrEP Adherence by Self-report. Trial comparisons, record NCT03070600-6eab54e2. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03070600-6eab54e2
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.472 | 0.423 | 0.521 | wilson | |
| Risk in group 2 | 0.375 | 0.324 | 0.429 | wilson | |
| Risk difference, group 1 minus group 2 | 0.0968 | 0.0237 | 0.168 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.26 | 1.05 | 1.5 | log | |
| Odds ratio, group 1 over group 2 | 1.49 | 1.1 | 2.01 | log | |
| Number needed to treat, for one more participant with the outcome on Universal Arm- PrEP Initiated than on Targeted Arm- PrEP Initiated | 10.3 | 5.95 | 42.2 | from the risk difference interval |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Universal Arm- PrEP Initiated | This analysis is restricted to participants who initiated PrEP during the study period. | 184 | 390 | OG000 |
| Group 2 | Targeted Arm- PrEP Initiated | This analysis is restricted to participants who initiated PrEP during the study period. | 120 | 320 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- OTHER_PRE_SPECIFIED
- Title
- PrEP Adherence by Self-report
- Description
- Any missed doses in the last month reported by participants
- Time frame
- Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).
- Population
Source ClinicalTrials.gov
Trial
- Title
- PrEP Implementation for Mothers in Antenatal Care
- NCT number
- NCT03070600
- Phases
- PHASE4
- Conditions
- HIV Infections, Pregnancy Related
- Interventions
- Universal PrEP Counseling, Targeted PrEP Counseling
- Lead sponsor
- University of Washington
- Results first posted
- 2022-05-10
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT03070600?tab=results
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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