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Oxygen Use Cohort vs No Oxygen Use Cohort: Number of Participants With Disease Progression From Index Date to Follow-up Forced Vital Capacity (FVC) Result

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

Measures 6

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

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.02330.02150.0253wilsonClinicalTrials.gov
Risk in group 20.01850.01690.0202wilsonClinicalTrials.gov
Risk difference, group 1 minus group 20.004820.00230.00735newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 21.261.121.42logClinicalTrials.gov
Odds ratio, group 1 over group 21.271.121.43logClinicalTrials.gov
Number needed to treat, for one more participant with the outcome on Oxygen Use Cohort than on No Oxygen Use Cohort207136435from the risk difference intervalClinicalTrials.gov

Groups 2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Oxygen Use CohortInterstitial lung disease (ILD) patients with ≥1 medical claim for oxygen therapy after fibrosing ILD diagnosis.57524,680OG000ClinicalTrials.gov
Group 2No Oxygen Use CohortPatients who were matched to a patient in the oxygen therapy cohort.45624,680OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypePRIMARYClinicalTrials.gov
TitleNumber of Participants With Disease Progression From Index Date to Follow-up Forced Vital Capacity (FVC) ResultClinicalTrials.gov
Description
The Number of participants with disease progression is reported instead of time to disease progression in the Outcome Measure Data Table.~Disease progression was defined as a 10% relative change between the index date to follow-up FVC result.
ClinicalTrials.gov
Time frameUp to month 12 of follow-up, in patient identification period from 01 October 2016 through 30 June 2022.ClinicalTrials.gov
Population
Among the 24,686 fibrosing Interstitial Lung Disease (ILD) patients who initiated oxygen therapy during the Aim 1 follow-up period, 24,680 were successfully matched at a 1:1 ratio with a fibrosing ILD patient who did not yet initiate oxygen therapy.~Patients of the matched cohort are included for which pre-index and follow-up forced vital capacity (FVC) results were available.
ClinicalTrials.gov

Trial 8

FieldValueSource
TitleOxygen Therapy Use in Patients With Fibrotic Interstitial Lung DiseaseClinicalTrials.gov
NCT numberNCT05957198ClinicalTrials.gov
PhasesClinicalTrials.gov
ConditionsLung Diseases, InterstitialClinicalTrials.gov
InterventionsClinicalTrials.gov
Lead sponsorBoehringer IngelheimClinicalTrials.gov
Results first posted2024-11-21ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT05957198?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.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.

ClinicalTrials.gov: none 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.