- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02198053
the Effect Between Platelet Reactivation and Antiplatelet Drugs
Effect of 180 mgTicagrelor Compared With 90 mg Ticagrelor on Platelet Reactivity in Patients Undergoing Elective PCI.
Study Overview
Status
Detailed Description
All admission patients were divided into two groups, the first group were prescribed loading dose (180 mg) ticagrelor, the second group were prescribed with 90 mg ticagrelor. We measured both platelet activity and platelet reactivity using the LTA at baseline, pre-operation and post-operation. All bleeding or dyspnea events were recorded in hospital period.
Primary endpoints: platelet activity, platelet reactivity using the LTA and safety events were recorded in hospital period.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
-
Beijing, China, 100029
- Anzhen Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
coronary artery disease, percutaneous coronary intervention
Exclusion Criteria:
high risk bleeding patient, allergic to the drugs
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Ticagrelor2
Ticagrelor with a loading dose of 180mg followed by 90 mg twice per day
|
|
Ticagrelor1
Ticagrelor with a dose of 90mg followed by 90 mg twice per day .
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Platelet reactivity
Time Frame: 1 year
|
LTA and TEG used to measure the effect of Platelet reactivity
|
1 year
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: LI QUAN, doctor, Beijing Anzhen Hospital
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- azliquan
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Drug Effect Disorder
-
Walter Reed National Military Medical CenterUnited States Department of Defense; General Services Administration (GSA)Active, not recruitingAdverse Drug Effect of Opioids | Adverse Drug Effect of BenzodiazepinesUnited States
-
Oslo University HospitalRecruiting
-
General Hospital of Ningxia Medical UniversityNot yet recruitingEffect of Drug | Adverse Effect of OpioidsChina
-
Boston Children's HospitalRecruiting
-
Boston Children's HospitalTerminatedDrug EffectUnited States
-
Suez Canal UniversityCompleted
-
Johns Hopkins UniversityNational Institute on Drug Abuse (NIDA)Completed
-
Services Institute of Medical Sciences, PakistanUnknown
-
Boston Children's HospitalRecruitingDrug EffectUnited States