Clinical Profile, Management Strategies, And Outcome Of Patients With Acute Chest Pain In Regional Referral Hospitals In Tanzania. Protocol For A Prospective, Multi-Centre Cohort Study
NCT ID: NCT06925568
Last Updated: 2025-04-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
317 participants
OBSERVATIONAL
2025-05-01
2026-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
\- Participants: Adults (18 years or older) who come to the ED with chest pain or suspected acute coronary syndrome (heart problem) at the regional referral hospitals in Dar es Salaam, Tanzania. Three regional referral hospitals and one specialized cardiac hospital (Jakaya Kikwete Cardiac Institute) will be involved in this study. Research assistants will collect data during routine care.
During the study, i. Enrollment will take place over 12 months; 317 patients with chest pain will be invited to participate.
ii. Researchers will record:
* How quickly patients receive initial diagnostic tests (e.g., ECG, blood tests for heart damage).
* Treatments given (e.g., medications, procedures to restore blood flow to the heart).
* Patient outcomes over 30 days (e.g., survival, readmission to the hospital, complications like another heart attack or stroke).
iii. Follow-up: Patients will be contacted by phone 30 days after their ED visit to check their health status.
This study is important because-: Chest pain is a common reason for ED visits, but in Tanzania, many patients face delays in diagnosis or lack access to lifesaving treatments. This study will identify gaps in care to help hospitals improve emergency services. Understanding the challenges in chest pain care can empower families to advocate for timely treatment for their loved ones. For Healthcare Providers: The findings will guide hospitals in adopting better protocols (e.g., faster ECGs, improved use of medications) and allocating resources effectively. For Policymakers: Results can inform national strategies to reduce deaths from heart disease in Tanzania.
During the study, participants should know that there will be no changes to care; patients will receive the same care they would normally get. The study only observes and records what happens. Personal information will be kept confidential, and data will be anonymized (no names or identifiers used). Participation is voluntary, and patients can choose to join or refuse without affecting their care.
Key Questions the Study Will Answer
1. How quickly do patients with chest pain get critical tests (like ECGs) and treatments in Tanzanian hospitals?
2. What are the most common barriers to timely care (e.g., lack of equipment, training gaps)?
3. What percentage of patients survive 30 days after a chest pain episode, and what factors influence their outcomes? Potential Benefits
* Improved Care: Findings may lead to better hospital protocols.
* Resource Allocation: Highlight where hospitals need more tools (e.g., ECG machines) or medications
* Global Impact: Lessons from Tanzania can help other low-resource countries improve emergency heart care.
Ethical Considerations
* Approval: The study has been reviewed and approved by ethics committees to ensure patient safety and rights.
* Informed Consent: Participants (or their families, if critically ill) will be asked for permission before joining.
How will results be shared-: Findings will be published in medical journals and shared with Tanzanian hospitals, health officials, and global organizations to drive improvements in emergency care.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Evaluation and Management of Patients With Acute Chest Pain in China
NCT02384863
ProspEctive First Evaluation in Chest Pain Trial
NCT01604655
Prognostic Accuracy of the HEART Score in Undifferentiated Chest Pain: A Multicenter Validation Study
NCT04580017
Retrospective Study of Acute Chest Pain in Extremely Critical Condition for More Than Ten Years
NCT02837120
Acute Coronary Syndrome KCMC
NCT04563546
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Patients above 18yrs presenting with acute chest pain or Suspected Acute Coronary Syndrome (ACS).
No Intervention: Observational Cohort
This is an observational study, so there is no direct intervention. However, the study involves documenting and analyzing the existing management strategies, including
* use of diagnostic tools ECG, troponin tests, etc
* Administration of medications such as antiplates and anticoagulants.
* Reperfusion therapies -thrombolysis, PCI
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
No Intervention: Observational Cohort
This is an observational study, so there is no direct intervention. However, the study involves documenting and analyzing the existing management strategies, including
* use of diagnostic tools ECG, troponin tests, etc
* Administration of medications such as antiplates and anticoagulants.
* Reperfusion therapies -thrombolysis, PCI
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
2. Lost to follow-up
3. The patient arrives in cardiac arrest.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Jakaya Kikwete Cardiac Institute
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Chiku Badru Mwimbo
Doctor
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
AB.123/307/01L/39
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.