Trial · NCT03615040
Results by group216
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 216
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Number of Moderate to Severe Exacerbation (Defined as Requiring Treatment With Systemic Corticosteroids and/or Antibiotics in the Community or Hospital or Hospitalisation). | Anti-ST2 | 2.21 | Standard Deviation 2.04 | Exacerbations | |
| Number of Moderate to Severe Exacerbation (Defined as Requiring Treatment With Systemic Corticosteroids and/or Antibiotics in the Community or Hospital or Hospitalisation). | Placebo | 2.67 | Standard Deviation 2.14 | Exacerbations | |
| Adverse Event Rate in the 48 Weeks of the Trial From First Dose | Anti-ST2 | 34 | Participants | ||
| Adverse Event Rate in the 48 Weeks of the Trial From First Dose | Placebo | 28 | Participants | ||
| Serious Adverse Event Rate in the 48 Weeks of the Trial From First Dose | Anti-ST2 | 12 | Participants | ||
| Serious Adverse Event Rate in the 48 Weeks of the Trial From First Dose | Placebo | 16 | Participants | ||
| St George's Respiratory Questionnaire for COPD Patients (SGRQ-C) Total Score | Anti-ST2 | Baseline | 60.1 | Standard Deviation 13.7 | score on a scale |
| St George's Respiratory Questionnaire for COPD Patients (SGRQ-C) Total Score | Placebo | Baseline | 58.4 | Standard Deviation 17.6 | score on a scale |
| St George's Respiratory Questionnaire for COPD Patients (SGRQ-C) Total Score | Anti-ST2 | Week 4 | 56.7 | Standard Deviation 13.5 | score on a scale |
| St George's Respiratory Questionnaire for COPD Patients (SGRQ-C) Total Score | Placebo | Week 4 | 58.9 | Standard Deviation 16.5 | score on a scale |
| St George's Respiratory Questionnaire for COPD Patients (SGRQ-C) Total Score | Anti-ST2 | Week 12 | 56.9 | Standard Deviation 15.2 | score on a scale |
| St George's Respiratory Questionnaire for COPD Patients (SGRQ-C) Total Score | Placebo | Week 12 | 59.9 | Standard Deviation 18.2 | score on a scale |
| St George's Respiratory Questionnaire for COPD Patients (SGRQ-C) Total Score | Anti-ST2 | Week 24 | 56.6 | Standard Deviation 15.3 | score on a scale |
| St George's Respiratory Questionnaire for COPD Patients (SGRQ-C) Total Score | Placebo | Week 24 | 59.6 | Standard Deviation 17.9 | score on a scale |
| St George's Respiratory Questionnaire for COPD Patients (SGRQ-C) Total Score | Anti-ST2 | Week 36 | 59.5 | Standard Deviation 14.6 | score on a scale |
| St George's Respiratory Questionnaire for COPD Patients (SGRQ-C) Total Score | Placebo | Week 36 | 59.5 | Standard Deviation 17.0 | score on a scale |
| St George's Respiratory Questionnaire for COPD Patients (SGRQ-C) Total Score | Anti-ST2 | Week 48 | 57.7 | Standard Deviation 15.7 | score on a scale |
| St George's Respiratory Questionnaire for COPD Patients (SGRQ-C) Total Score | Placebo | Week 48 | 63.3 | Standard Deviation 17.2 | score on a scale |
| COPD Assessment Test (CAT) (Questionnaire) | Anti-ST2 | Week 0 | 22.1 | Standard Deviation 6.6 | score on a scale |
| COPD Assessment Test (CAT) (Questionnaire) | Placebo | Week 0 | 22.6 | Standard Deviation 5.7 | score on a scale |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
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
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
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GET https://conductscience.org/api/trials/v1/NCT03615040/results