Comparison · NCT05236725-sae
Remote Blood Pressure Monitoring (rBPM) vs Standard of Care (SOC): serious adverse events
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. Remote Blood Pressure Monitoring (rBPM) vs Standard of Care (SOC): serious adverse events. Trial comparisons, record NCT05236725-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05236725-sae
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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 | 0.0467 | 0.0336 | 0.0646 | wilson | |
| Risk in group 2 | 0.0326 | 0.0224 | 0.0474 | wilson | |
| Risk difference, group 1 minus group 2 | 0.0141 | -0.00564 | 0.0347 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.43 | 0.868 | 2.36 | log | |
| Odds ratio, group 1 over group 2 | 1.45 | 0.863 | 2.45 | log | |
| Number needed to harm, for one more participant with a serious adverse event on Remote Blood Pressure Monitoring (rBPM) than on Standard of Care (SOC) | 71 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: standard of care.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Remote Blood Pressure Monitoring (rBPM) | Subjects randomized to rBPM arm receive the appropriate standard of care depending upon their risk level, as well as the remote BP monitoring app (BabyScripts) and Bluetooth enabled BP cuff/monitor, and will receive the following equipment and monitoring:~* a specialized, Bluetooth enabled BP monitoring cuff (Clinically Validated, A\&D Medical Wireless Blood Pressure Monitor-Upper Arm (Appendix 2)~* BP monitoring smart phone app, BabyScripts™~* Verbal and written instructions, to conduct BP checks at home | 34 | 728 | EG001 |
| Group 2 | Standard of Care (SOC) | Subjects randomized to SOC arm are provided with the appropriate standard of care depending upon their risk level (as determined by their individual provider or WFBMC Maternal-Fetal Medicine provider) | 26 | 797 | EG000 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
All adverse events excluding severe hypertensive events were assessed from the time of hospital discharge through 8 weeks (56 days) postpartum. For severe hypertensive events, systolic and diastolic blood pressure measurements were evaluated from discharge through 3 weeks (21 days) postpartum.
Source ClinicalTrials.gov
Trial
- Title
- Monitoring and Testing of Blood Pressure in Postpartum Women
- NCT number
- NCT05236725
- Phases
- NA
- Conditions
- Hypertension
- Interventions
- Remote Blood Pressure Cuff, Blood pressure monitoring smart phone app, BabyScripts™, Instructions
- Lead sponsor
- Wake Forest University Health Sciences
- Results first posted
- 2026-03-02
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT05236725?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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