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NCT05960474 · ClinicalTrials.gov registry record

Coronary Microvascular Disease (CMD) Registry

A clinical trial of Coronary Microvascular Dysfunction, sponsored by Medstar Health Research Institute.

Recruiting
Registry status
1,000
Enrollment target
3
Study locations

NCT05960474: Recruiting study of Coronary Microvascular Dysfunction, sponsored by Medstar Health Research Institute.

NCT05960474 is a study of Coronary Microvascular Dysfunction that is actively recruiting participants, run by Medstar Health Research Institute. The registered enrollment target is 1,000 participants, above the 129-participant average among 7 other Coronary Microvascular Dysfunction trials with a reported enrollment target (675% higher). The trial reports 3 study locations across 3 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05960474, a study of Coronary Microvascular Dysfunction, is actively recruiting participants, sponsored by Medstar Health Research Institute.

RECRUITING
Registry status
1,000 participants
Enrollment target
3
Study locations

Study Summary

The purpose of this project is to provide appropriate administrative and technical supports for the warehousing and use of a database of patients with coronary microvascular disease (CMD). This protocol will outline the process for identification and capture of data, storage, as well as data use and sharing internally and externally for research purposes.

Interventions

  • OTHER Outcomes for Patients with CMD

Study Locations (3)

District of Columbia

  • Medstar Washington Hospital Center - Washington D.C.

Florida

  • Memorial Regional Hospital - Hollywood

Maryland

  • MedStar Southern Maryland - Clinton

Trial Details

FieldValue
Enrollment Target 1,000 participants
Start Date 2023-02-01
Est. Completion 2033-01
Medstar Health Research Institute

115 total trials

What NCT05960474 shows while recruiting

NCT05960474 is an observational study that tracks outcomes without assigning an intervention. Its 1,000 participants enrollment target places it among the larger protocols in the corpus, above the 129-participant average among 7 other Coronary Microvascular Dysfunction trials with a reported enrollment target (675% higher).

The record links to 1 condition, with Coronary Microvascular Dysfunction appearing as the primary indexed condition, and to 1 intervention - of which Outcomes for Patients with CMD is the first listed.

NCT05960474 reports a single indexed study location in District of Columbia, Florida, Maryland.

Frequently Asked Questions

What is clinical trial NCT05960474 about?

NCT05960474 is a clinical study titled "Coronary Microvascular Disease (CMD) Registry". The purpose of this project is to provide appropriate administrative and technical supports for the warehousing and use of a database of patients with coronary microvascular disease (CMD). This protocol will outline the process for identification and capture of data, storage, as well as data use and...

What is the current status of trial NCT05960474?

This trial is currently recruiting. The enrollment target is 1,000 participants. The study started on 2023-02-01. Estimated completion is 2033-01.

What conditions does trial NCT05960474 study?

This clinical trial studies the following conditions: Coronary Microvascular Dysfunction.

What interventions are being tested in trial NCT05960474?

The interventions under investigation include: Outcomes for Patients with CMD (OTHER).

Who is sponsoring clinical trial NCT05960474?

This trial is sponsored by Medstar Health Research Institute, which has 115 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05960474 being conducted?

This trial has 3 study locations across District of Columbia, Florida, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT05960474, the US trial registry maintained by the National Library of Medicine. NCT05960474 (large enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.