Clinical TrialID 3559

Study of Policosanol to Improve Platelet Reactivity After Percutaneous Coronary Stent Implantation (PCI)

NCT01371058

Coronary Artery Disease

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Record Fields

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Clinical Trial Id
3559
Evidence Id
3559
Core Evidence Id
3559
Source Clinical Trial Id
3533
Herb2 Clinical Trial Id
HBCT003533
Nct Id
NCT01371058
Title
Study of Policosanol to Improve Platelet Reactivity After Percutaneous Coronary Stent Implantation (PCI)
Status
Completed
Phase
Phase 4
Study Result
No
Study Condition
Coronary Artery Disease
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: PREVENTION
Intervention
DRUG: high maintenance clopidogrel|DRUG: routine dual antiplatelet|DRUG: policosanol plus dual antiplatelet
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Intervention Purpose
Prevention
Gender
All
Age
Adult, Older_Adult
Enrollment
350
Outcome Measure
reversion rate of HPR, reversion was defined as platelet aggregation \<65%, 30 days
Sponsor Collaborator
Shenyang Northern Hospital
Funded By
OTHER
Location
The First Hospital of China Medical University, Shenyang, Liaoning, 110001, China
Other Id
NH-20110530
Start Date
2011-03
Primary Completion Date
2012-09
Completion Date
2013-09
First Posted
2011-06-10
Results First Posted
Last Update Posted
2015-12-16
Study Document
Study Url
https://clinicaltrials.gov/study/NCT01371058
Title Cn
Title En
Study of Policosanol to Improve Platelet Reactivity After Percutaneous Coronary Stent Implantation (PCI)
Bilingual Status
semi_complete