Trial · NCT02173379
Outcomes169
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 20 of 169
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Number of Participants With Target Lesion Failure (TLF) | 30 days | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | TLF at 1-year, Non-inferiority Against the Control | 1 year | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Angina at 1-year, Non-inferiority Against the Control | 1 year | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Percentage of Target Lesion With Acute Success- Device Success (Lesion Level Analysis) | In-hospital (≤ 7days) | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Percentage of target lesions | NUMBER |
| SECONDARY | Number of Participants With Acute Success- Procedural Success (Subject Level Analysis) | In-hospital (≤ 7days) | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Death (Cardiac, Vascular, Non-cardiovascular) | In-hospital (≤ 7 days post index procedure) | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Death (Cardiac, Vascular, Non-cardiovascular) | 30 days | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Death (Cardiac, Vascular, Non-cardiovascular) | 90 days | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Death (Cardiac, Vascular, Non-cardiovascular) | 180 days | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Death (Cardiac, Vascular, Non-cardiovascular) | 270 days | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Death (Cardiac, Vascular, Non-cardiovascular) | 1 year | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Death (Cardiac, Vascular, Non-cardiovascular) | 2 years | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Death (Cardiac, Vascular, Non-cardiovascular) | 3 years | ITT population. The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Death (Cardiac, Vascular, Non-cardiovascular) | 4 years | ITT population. The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Death (Cardiac, Vascular, Non-cardiovascular) | 5 years | ITT population. The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With Myocardial Infarction (MI) | In-hospital (≤ 7 days post index procedure) | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With Myocardial Infarction (MI) | 30 days | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With Myocardial Infarction (MI) | 90 days | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With Myocardial Infarction (MI) | 180 days | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With Myocardial Infarction (MI) | 270 days | ITT population.The number of participants analyzed includes subjects who had available follow up data at that time frame. | Participants | COUNT_OF_PARTICIPANTS |
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.
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GET https://conductscience.org/api/trials/v1/NCT02173379/outcomes