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Evaluation of Emotional Status and Coronary Flow Characteristics by TIMI Frame Count Method

Effects of Emotional Status on Coronary Flow in Patients Undergoing Coronary Angiography:Multicenter TIMI Frame Count Assessment Study (STRAIN-TIMI Study)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02831153
Acronym
STRAIN-TIMI
Enrollment
2000
Registered
2016-07-13
Start date
2016-07-31
Completion date
2017-07-31
Last updated
2016-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Coronary Artery Disease, Coronary Artery Ectasia, Depression, Endothelial Dysfunction, Slow-Flow Phenomenon

Brief summary

This study evaluates the effects of emotional status on coronary flow in patients undergoing elective coronary angiography. Patients whom undergoing elective coronary angiography will fulfill the Beck Anxiety Inventory, Beck Depression Inventory, State-Trait Anxiety Inventory, Hospital Anxiety and Depression Scale. State Anxiety Inventory will be fulfilled both before the intervention and after 1 hour the patients learned the results of the coronary angiography. The other scales will be performed after 1 hour the patients learned their results. Coronary flow will be assessed by TIMI (Thrombolysis In Myocardial Infarction) frame count method.

Interventions

PROCEDUREcoronary angiography

Coronary angiography will be performed by transfemoral or transradial approach in all patients. In order to evaluate each coronary artery, at least four views from the left and two views from the right system will be taken.

Sponsors

Abant Izzet Baysal University
CollaboratorOTHER
Saglik Bilimleri Universitesi Gulhane Tip Fakultesi
CollaboratorOTHER
Ankara City Hospital Bilkent
CollaboratorOTHER
Private Yenisehir Hospital
CollaboratorUNKNOWN
Private Gozde Hospital
CollaboratorUNKNOWN
Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital
CollaboratorOTHER
Ertan YETKIN
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
TRIPLE (Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients whom planned elective coronary angiography and accept to be included in the study as a participant

Exclusion criteria

* \< 18 years, history of prior coronary angiography, history of coronary artery revascularization, acute coronary syndrome patients, atrial fibrillation, heart failure, known systemic diseases

Design outcomes

Primary

MeasureTime frame
TIMI frame count method analysis1 day

Countries

Turkey (Türkiye)

Contacts

Primary ContactErtan Yetkin, MD
ertanyetkin@hotmail.com905327136721
Backup ContactSelcuk Ozturk, MD
selcukozturk85@hotmail.com905535376613

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026