The Pharmacogenetics of Optimal Warfarin Therapy in Chinese Patients After Heart Valve Replacement. (POWAT)
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ClinicalTrials.gov Identifier: NCT02710747 |
Recruitment Status : Unknown
Verified December 2015 by Guangdong Provincial People's Hospital.
Recruitment status was: Recruiting
First Posted : March 17, 2016
Last Update Posted : March 17, 2016
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To value the accuracy of the dosing algorithm published by the International Warfarin Pharmacogenetics Consortium in Chinese patients after heart valve replacement.
To value the accuracy of warfarin pharmacogenomics algorithm by the algorithm calculated dose and actual dose in the Chinese patients.
Condition or disease | Intervention/treatment | Phase |
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Heart Valve Disease Older Than 18-years-old Without Any Liver or Kidney Diseases | Genetic: CYP2C9;VKORC1 | Phase 4 |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 500 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Double (Participant, Care Provider) |
Primary Purpose: | Treatment |
Official Title: | The Pharmacogenetics of Optimal Warfarin Therapy in Chinese Patients After Heart Valve Replacement. |
Study Start Date : | January 2015 |
Estimated Primary Completion Date : | June 2016 |
Estimated Study Completion Date : | July 2016 |

Arm | Intervention/treatment |
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Experimental: Genetic Group
Dose (mg/week) = [5.6044 - 0.02614 × Age [in years] + 0.0087 × Height [cm] + 0.0128 × Weight [kg] - 0.8677 × VKORC1 A/G -1.6974 × VKORC1 A/A - 0.5211 × CYP2C9 *1/*2 - 0.9357 × CYP2C9 *1/*3 - 1.0616 × CYP2C9 *2/*2 - 1.9206 × CYP2C9*2/*3 - 2.3312 × CYP2C9 *3/*3 - 0.1092 × Asian race - 0.5503 × amiodarone ]2
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Genetic: CYP2C9;VKORC1 |
No Intervention: Control Group
Dose for the first three days after operation will be 4.5mg/d.
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- The perccentage of time that the INR was in the therapeutic range [ Time Frame: 3 months ]
- all drainage fluid of every patient [ Time Frame: 1 week after operation ]

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Ages Eligible for Study: | 18 Years to 80 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:atrial fibrillation
- atrial fibrillation
- heart valve replacement
- VTE
Exclusion Criteria:
- severe liver or kidney diseases

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02710747
Contact: Chen Yongbin, master | +8618688859129 | chenyb1020@hotmail.com |
China, Guangdong | |
Guangdong General Hospital | Recruiting |
Guangzhou, Guangdong, China, 510080 | |
Contact: Chen Yongbin, Master +8618688859129 chenyb1020@hotmail.com |
Responsible Party: | Guangdong Provincial People's Hospital |
ClinicalTrials.gov Identifier: | NCT02710747 History of Changes |
Other Study ID Numbers: |
GDREC2014265H |
First Posted: | March 17, 2016 Key Record Dates |
Last Update Posted: | March 17, 2016 |
Last Verified: | December 2015 |
warfarin Chinese patients heart valve replacement |
Kidney Diseases Heart Valve Diseases Urologic Diseases Heart Diseases |
Cardiovascular Diseases Warfarin Anticoagulants |