Clinical Trials Directory

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

TypeNameDescription
OTHERantidepressive and anti-anxiety therapyThese 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.