Trial · NCT03985943
Outcomes18
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 18 of 18
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Percentage of Participants With an Investigator's Global Assessment (IGA) Success (IGA of 0 or 1 and a More Than Equal to [>=] 2-point Reduction): Intent-To-Treat (ITT) Population | Week 16 | The ITT population consisted of all randomized participants. Data was planned to be collected and analyzed for Initial Treatment Period. | percentage of participants | NUMBER |
| PRIMARY | Percentage of Participants With an Investigator's Global Assessment (IGA) Success (IGA of 0 or 1 and a >= 2-point Reduction): Severe Pruritus Population | Week 16 | Severe pruritus population consisted of all randomized participants with a baseline PP NRS \>=7. Data was planned to be collected and analyzed for Initial Treatment Period. | percentage of participants | NUMBER |
| PRIMARY | Percentage of Participants With >=75% Improvement in Eczema Area and Severity Index (EASI-75) at Week 16: ITT Population | Week 16 | The ITT population consisted of all randomized participants. Data was planned to be collected and analyzed for Initial Treatment Period. | percentage of participants | NUMBER |
| PRIMARY | Percentage of Participants With >=75% Improvement in Eczema Area and Severity Index (EASI-75) at 16: Severe Pruritus Population | Week 16 | Severe pruritus population consisted of all randomized participants with a baseline PP NRS \>=7. Data was planned to be collected and analyzed for Initial Treatment Period. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants With Improvement of >=4 Points in Weekly Average Peak Pruritus Numeric Rating Scale (PP NRS) at Week 16: ITT Population | Week 16 | The ITT population consisted of all randomized participants. Data was planned to be collected and analyzed for Initial Treatment Period. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants With Improvement of >=4 Points in Weekly Average Peak Pruritus Numeric Rating Scale (PP NRS) at Week 16: Severe Pruritus Population | Week 16 | Severe pruritus population consisted of all randomized participants with a baseline PP NRS \>=7. Data was planned to be collected and analyzed for Initial Treatment Period. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants With <2 Points in Weekly Average PP NRS at Week 16: ITT Population | Week 16 | The ITT population consisted of all randomized participants. Data was planned to be collected and analyzed for Initial Treatment Period. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants With <2 Points in Weekly Average PP NRS at Week 16: Severe Pruritus Population | Week 16 | Severe pruritus population consisted of all randomized participants with a baseline PP NRS \>=7. Data was planned to be collected and analyzed for Initial Treatment Period. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants With an Improvement of Sleep Disturbance Numeric Rating Scale (SD NRS) >=4 at Week 16: ITT Population | Week 16 | The ITT population consisted of all randomized participants. | percentage of subjects | NUMBER |
| SECONDARY | Percentage of Participants With an Improvement of Sleep Disturbance Numeric Rating Scale (SD NRS) >=4 at Week 16: Severe Pruritus Population | Week 16 | Severe pruritus population consisted of all randomized participants with a baseline PP NRS \>=7. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants With Improvement of >=4 Points in Weekly Average Peak Pruritus Numeric Rating Scale (PP NRS) at Week 4: ITT Population | Week 4 | The ITT population consisted of all randomized participants. Data was planned to be collected and analyzed for Initial Treatment Period. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants With Improvement of >=4 Points in Weekly Average Peak Pruritus Numeric Rating Scale (PP NRS) at Week 4: Severe Pruritus Population | Week 4 | Severe pruritus population consisted of all randomized participants with a baseline PP NRS \>=7. Data was planned to be collected and analyzed for Initial Treatment Period. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants With Peak Pruritus Numeric Rating Scale (PP NRS) <2 at Week 4: ITT Population | Week 4 | The ITT population consisted of all randomized participants. Data was planned to be collected and analyzed for Initial Treatment Period. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants With Peak Pruritus Numeric Rating Scale (PP NRS) <2 at Week 4: Severe Pruritus Population | Week 4 | Severe pruritus population consisted of all randomized participants with a baseline PP NRS \>=7. Data was planned to be collected and analyzed for Initial Treatment Period. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants With Improvement of >=4 Points in Weekly Average Peak Pruritus Numeric Rating Scale (PP NRS) at Week 2: ITT Population | Week 2 | The ITT population consisted of all randomized participants. Data was planned to be collected and analyzed for Initial Treatment Period. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants With Improvement of >=4 Points in Weekly Average Peak Pruritus Numeric Rating Scale (PP NRS) at Week 2: Severe Pruritus Population | Week 2 | Severe pruritus population consisted of all randomized participants with a baseline PP NRS \>=7. Data was planned to be collected and analyzed for Initial Treatment Period. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants With Improvement of >=4 Points in Weekly Average Peak Pruritus Numeric Rating Scale (PP NRS) at Week 1: ITT Population | Week 1 | The ITT population consisted of all randomized participants. Data was planned to be collected and analyzed for Initial Treatment Period. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants With Improvement of >=4 Points in Weekly Average Peak Pruritus Numeric Rating Scale (PP NRS) at Week 1: Severe Pruritus Population | Week 1 | Severe pruritus population consisted of all randomized participants with a baseline PP NRS \>=7. Data was planned to be collected and analyzed for Initial Treatment Period. | percentage of participants | NUMBER |
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/NCT03985943/outcomes