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NCT05777590 · ClinicalTrials.gov registry record
Comparison of ICG Microangiography and Conventional Angiography in Severe Frostbite
A clinical trial of Frostbite, sponsored by HealthPartners Institute.
- Active
- Registry status
- 8
- Enrollment target
- 1
- Study location
NCT05777590: Active study of Frostbite, sponsored by HealthPartners Institute.
NCT05777590 is a study of Frostbite that is active but no longer recruiting, run by HealthPartners Institute. The registered enrollment target is 8 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05777590, a study of Frostbite, is active but no longer recruiting, sponsored by HealthPartners Institute.
- ACTIVE NOT RECRUITING
- Registry status
- 8 participants
- Enrollment target
- 1
- Study location
Study Summary
Severe frostbite injury is a significant cause of morbidity in northern climates. Minnesota has some of the highest numbers of severe frostbite injuries in North America. As a result, Regions Hospital has the best opportunity to study this disease process and improve outcomes for frostbite patients. The diagnostic methods for severe frostbite injury vary from institution to institution and there is no standard practice. Commonly utilized methods include conventional angiography, Technetium 99 triple phase bone scans, SPECT studies, Indocyanine Green microangiography, and doppler studies. The proposed pilot study aims to directly compare conventional angiography imaging to ICG microangiography in adult patients with severe frostbite. Severe frostbite is defined as 4th degree: frostbite resulting in vascular occlusion and tissue ischemia. Both imaging modalities have been used for the diagnosis and monitoring of severe frostbite injury but there has never been a study directly comparing these two imaging modalities.
Primary Outcome
Hypothesize that these two imaging modalities (ICG (indocyanine green) and conventional angiography) will be concordant at demonstrating the ischemic tissue present in severe frostbite.
Conditions Studied
Interventions
- DRUG Indocyanine Green Angiogram
Study Locations (1)
Minnesota
- Regions Hospital - Saint Paul
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 8 participants |
| Start Date | 2023-02-03 |
| Est. Completion | 2026-05-30 |
What the registry record for NCT05777590 still lists
NCT05777590 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 8 participants, a relatively small participant target.
The record links to 1 condition, with Frostbite appearing as the primary indexed condition, and to 1 intervention - of which Indocyanine Green Angiogram is the first listed.
NCT05777590 reports a single indexed study location in Minnesota.
Frequently Asked Questions
What is clinical trial NCT05777590 about?
NCT05777590 is a clinical study titled "Comparison of ICG Microangiography and Conventional Angiography in Severe Frostbite". Severe frostbite injury is a significant cause of morbidity in northern climates. Minnesota has some of the highest numbers of severe frostbite injuries in North America. As a result, Regions Hospital has the best opportunity to study this disease process and improve outcomes for frostbite patients....
What is the current status of trial NCT05777590?
This trial is currently active not recruiting. The enrollment target is 8 participants. The study started on 2023-02-03. Estimated completion is 2026-05-30.
What conditions does trial NCT05777590 study?
This clinical trial studies the following conditions: Frostbite.
What interventions are being tested in trial NCT05777590?
The interventions under investigation include: Indocyanine Green Angiogram (DRUG).
Who is sponsoring clinical trial NCT05777590?
This trial is sponsored by HealthPartners Institute, which has 146 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05777590 being conducted?
This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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