Trials / Unknown
UnknownNCT03057691
The Impact of Depression and/or Anxiety on PCI Patients
The Impact of Depression and/or Anxiety on Patients With Acute Coronary Syndrome After Percutaneous Coronary Interventions
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 5,000 (estimated)
- Sponsor
- First Affiliated Hospital Xi'an Jiaotong University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate how depression and/or anxiety could effect the prognosis of the patients post-ACS after PCI.
Detailed description
This trial is a prospective, multi-centric, real-world clinical study. About 5,000 patients with ACS post-PCI will be recruited according to the resource available of each participating center to represent real-world setting. Patients enrolled in the project will accept two-years' follow-up and will be assessed on mortality, cardiovascular events, and severity of depressive or anxiety symptoms using self-rating scales continuously during the trial, in which their treatment for anxiety or depression will also be documented.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | antidepressive and anti-anxiety therapy | These therapies include antidepressants, antianxiety drugs and psychotherapy. Subjects choose the therapy follow their own will. All of the above-mentioned therapies are identified by experienced psychiatrists in the same center. The treatment information will be recorded in each visit. The study is considered non-interventional, and no antidepressive or anti-anxiety therapies are mandated. |
Timeline
- Start date
- 2017-03-11
- Primary completion
- 2019-12-01
- Completion
- 2020-01-01
- First posted
- 2017-02-20
- Last updated
- 2018-11-16
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT03057691. Inclusion in this directory is not an endorsement.