Trials / Unknown
UnknownNCT03413410
A Multi-Center Study on the Metoprolol Optimal Dosing Pathway of Metoprolol Application in Chinese Patients With Acute Coronary Syndrome
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 1,000 (estimated)
- Sponsor
- Yun Dai Chen · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
This study is to test the feasibility and tolerability of the metoprolol optimal dosing pathway by observing the percentage of patients achieving target dose followed the pathway on ACS patients during hospitalization.
Detailed description
Acute coronary syndrome(ACS) is one of the main manifestations of cardiovascular disease and one of the main causes for hospitalization in adults. Previous studies showed that β-receptor blockers can reduce ACS patients' cardiovascular risk in both acute phase and secondary prevention. We summarized the metoprolol optimal dosing pathway based on Chinese and foreign guidelines as well as Chinese clinical practice. Primary endpoint is the percentage of patients achieving target dose at time of discharge. Secondary endpoints are the mean HR \& BP at discharge and during the follow up period of the Patients who have achieved target dose at discharge.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Metoprolol | Patients with acute coronary syndrome take metoprolol during hospital and after discharge in the optimal dosing pathway. |
Timeline
- Start date
- 2018-02-01
- Primary completion
- 2019-07-30
- Completion
- 2020-07-30
- First posted
- 2018-01-29
- Last updated
- 2019-07-19
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT03413410. Inclusion in this directory is not an endorsement.