ConductScience.org, home

Comparison · NCT02995733-sae

PARTICS vs Usual Care: serious adverse events

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

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

Download JSON
Cite this record

ConductScience Library. PARTICS vs Usual Care: serious adverse events. Trial comparisons, record NCT02995733-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02995733-sae

On this page

Measures6

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

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.1230.09940.152wilson
Risk in group 20.1210.09760.149wilson
Risk difference, group 1 minus group 20.00204-0.03490.039newcombe hybrid score
Risk ratio, group 1 over group 21.020.7531.37log
Odds ratio, group 1 over group 21.020.7231.44log
Number needed to harm, for one more participant with a serious adverse event on PARTICS than on Usual Care490from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: usual care.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1PARTICS
addition of PARTICS strategy - Patient Activated Reliever-Triggered Inhaled CorticoSteroid (PARTICS) using QVAR . Patient will use inhaled corticosteroid at time of rescue inhaler use~PARTICS using QVAR: Patient takes inhaled corticosteroid at the time of rescue inhaler use
75609EG000
Group 2Usual CareProvider-enhanced usual care arm; no change in asthma management74611EG001

Harm

What it counts
Total, serious adverse events
Time frame
From enrollment to study completion, an average of 15 months per participant.

Source ClinicalTrials.gov

Trial

Title
Patient Empowered Strategy to Reduce Asthma Morbidity in Highly Impacted Populations; PeRson EmPowered Asthma RElief
NCT number
NCT02995733
Phases
PHASE4
Conditions
Asthma
Interventions
PARTICS using QVAR
Lead sponsor
Brigham and Women's Hospital
Results first posted
2023-01-19

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.

For software

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT02995733-sae