NCT05303441

Brief Summary

Our study is planning to evaluate patients with chronic kidney disease who come to the emergency department with chest pain. Estimated GFR (cisGFR) with cystatin and estimated GFR (creaGFR) with creatinine will be calculated. Symptoms, ECG and troponin values of patients will be evaluated for diagnosis of acute coronary syndrome

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
172

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Mar 2022

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 7, 2022

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

March 9, 2022

Completed
22 days until next milestone

First Posted

Study publicly available on registry

March 31, 2022

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 7, 2023

Completed
25 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2023

Completed
Last Updated

March 31, 2022

Status Verified

March 1, 2022

Enrollment Period

10 months

First QC Date

March 9, 2022

Last Update Submit

March 29, 2022

Conditions

Outcome Measures

Primary Outcomes (2)

  • anticipated ACS

    The role of cystatin C in diagnosis acute coronary syndrome when used with troponin in patients with chronic renal failure.

    time passed until PCI (percutaneous coronary intervention) (pre-intervention) or admission to hospital

  • exclusion of acs

    exclusion of ACS according to current guidelines

    time passed during emergency department visit until discharge avarage of 3-6 hours

Study Arms (2)

patients with acute coronary syndrome

patients with chronic kidney disease having chest pain with ecg, symptom or cardiac troponin levels compatible with ACS

Procedure: percutaneous coronary intervention

patients without acute coronary syndrome

patients with chronic kidney disease having chest pain with ecg, symptom or cardiac troponin levels NONcompatible with ACS

Interventions

conventional coronary angiography

patients with acute coronary syndrome

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

patients with chronic kidney disease having chest pain and administered to emergency department for differential diagnosis of chest pain or equivalent of chest pain (dyspnea, diaphoresis, syncope, nausea, vomiting)

You may qualify if:

  • Age over 18,
  • chronic kidney diease having chest pain or equivalent of chest pain (dyspnea, diaphoresis, syncope, nausea, vomiting) -

You may not qualify if:

  • STEMI,
  • age less than 18,
  • missing data,
  • patients referred to or accepted from another medical facility

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Diskapi Research and Training Hospital

Ankara, 06110, Turkey (Türkiye)

RECRUITING

Related Publications (1)

  • Hamzacebioglu E, Sonmez BM, Akcay G, Tulmac M, Kayisoglu S, Hatil SI, Gungor EB. Valency of cystatin C and creatinine on troponin values in chronic kidney disease patients with chest pain in emergency department. Am J Emerg Med. 2025 Mar;89:95-102. doi: 10.1016/j.ajem.2024.12.020. Epub 2024 Dec 13.

MeSH Terms

Conditions

Acute Coronary SyndromeRenal Insufficiency, Chronic

Interventions

Percutaneous Coronary Intervention

Condition Hierarchy (Ancestors)

Myocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular DiseasesRenal InsufficiencyKidney DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Endovascular ProceduresVascular Surgical ProceduresCardiovascular Surgical ProceduresSurgical Procedures, OperativeMinimally Invasive Surgical Procedures

Study Officials

  • bedriye müge sönmez, assoc. prof.

    research

    STUDY DIRECTOR

Central Study Contacts

bedriye müge sönmez, assoc. prof.

CONTACT

elif hamzaçebioğlu, resident

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
associate professor

Study Record Dates

First Submitted

March 9, 2022

First Posted

March 31, 2022

Study Start

March 7, 2022

Primary Completion

January 7, 2023

Study Completion

February 1, 2023

Last Updated

March 31, 2022

Record last verified: 2022-03

Locations