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Comparison · NCT03984188-deaths

Low-dose Theophylline Group vs Placebo Group: deaths from any cause

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. Low-dose Theophylline Group vs Placebo Group: deaths from any cause. Trial comparisons, record NCT03984188-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03984188-deaths

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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 10.040.0110.135wilson
Risk in group 20.08160.03220.192wilson
Risk difference, group 1 minus group 2-0.0416-0.1560.0651newcombe hybrid score
Risk ratio, group 1 over group 20.490.0942.55log
Odds ratio, group 1 over group 20.4690.08182.69log
Number needed to treat, for one fewer death from any cause on Low-dose Theophylline Group than on Placebo Group24from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Low-dose Theophylline Group
Participant in this group will receive low-dose theophylline in addition to standard care, per World Health Organization (WHO) guidelines for management of Chronic Obstructive Pulmonary Disease (COPD) treatment, over a one year period.~Theophylline ER: 200 mg extended release (ER) low-dose theophylline taken orally daily~Standard of Care Treatment: Per World Health Organization (WHO) guidelines for management of Chronic Obstructive Pulmonary Disease (COPD) treatment
250EG000
Group 2Placebo Group
Participant in this group will receive a placebo in addition to standard care, per World Health Organization (WHO) guidelines for management of Chronic Obstructive Pulmonary Disease (COPD) treatment.~Placebo oral tablet: Manufactured methylcellulose placebo tablet taken orally daily~Standard of Care Treatment: Per World Health Organization (WHO) guidelines for management of Chronic Obstructive Pulmonary Disease (COPD) treatment
449EG001

Harm

What it counts
Total, all-cause mortality
Time frame
1 year

Source ClinicalTrials.gov

Trial

Title
Effectiveness of Low-Dose Theophylline for the Management of Biomass-Associated COPD
NCT number
NCT03984188
Phases
PHASE3
Conditions
COPD, COPD Exacerbation, COPD Exacerbation Acute, Pollution Related Respiratory Disorder, Pollution; Exposure
Interventions
Theophylline ER, Placebo oral tablet, Standard of Care Treatment
Lead sponsor
University of Miami
Results first posted
2024-10-29

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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