Effect of Fire Suppression and Emergency Duties on Vascular Function
NCT ID: NCT01805063
Last Updated: 2024-05-01
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
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COMPLETED
30 participants
OBSERVATIONAL
2012-01-09
2016-12-31
Brief Summary
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The investigators hypothesize that participation in active fire-fighting duties impairs blood vessel function and increases blood clot formation when compared with non-fire-fighting activities. In this study, healthy career firefighters will be assessed after three periods of duty: fire-suppression, emergency response without fire suppression and following a sedentary shift. The investigators will take blood samples to measure platelet activity (platelets are the particles in blood that help blood clot) and will examine how blood clots outside of the body. The investigators will then perform studies placing small needles in the arm to assess blood vessel function following these duties. By undertaking this comprehensive assessment of blood, blood vessel and heart function the investigators hope to understand the mechanisms whereby the risk of a heart attack, fatal or otherwise, is posed throughout these distinct duties that firefighters undertake on a daily basis.
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Detailed Description
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Conditions
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Study Design
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CASE_CROSSOVER
PROSPECTIVE
Study Groups
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Fire suppression
Firefighters will attend for vascular assessments following a night shift where they have performed fire suppression
Forearm Vascular Study
Forearm venous occlusion plethysmography to measure forearm blood flow during intra-arterial infusion of the vasodilators Verapamil (10-100 µg/min), bradykinin (100-1000 pmol/min), sodium nitroprusside (2-8 µg/min) and Acetylcholine (5-20 µg/min).
Badimon Chamber
Ex-vivo assessment of thrombus formation using the Badimon Chamber
Non-fire emergency duty
Firefighters will attend for vascular assessments following a night shift where they have had an emergency response without fire suppression eg. road traffic collision.
Forearm Vascular Study
Forearm venous occlusion plethysmography to measure forearm blood flow during intra-arterial infusion of the vasodilators Verapamil (10-100 µg/min), bradykinin (100-1000 pmol/min), sodium nitroprusside (2-8 µg/min) and Acetylcholine (5-20 µg/min).
Badimon Chamber
Ex-vivo assessment of thrombus formation using the Badimon Chamber
Sedentary shift
Firefighters will attend for vascular assessments following a night shift where they have remained sedentary throughout the shift.
Forearm Vascular Study
Forearm venous occlusion plethysmography to measure forearm blood flow during intra-arterial infusion of the vasodilators Verapamil (10-100 µg/min), bradykinin (100-1000 pmol/min), sodium nitroprusside (2-8 µg/min) and Acetylcholine (5-20 µg/min).
Badimon Chamber
Ex-vivo assessment of thrombus formation using the Badimon Chamber
Interventions
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Forearm Vascular Study
Forearm venous occlusion plethysmography to measure forearm blood flow during intra-arterial infusion of the vasodilators Verapamil (10-100 µg/min), bradykinin (100-1000 pmol/min), sodium nitroprusside (2-8 µg/min) and Acetylcholine (5-20 µg/min).
Badimon Chamber
Ex-vivo assessment of thrombus formation using the Badimon Chamber
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* History of lung or ischaemic heart disease
* Malignant arrhythmia
* Systolic blood pressure \>190mmHg or \<100mmHg
* Renal or hepatic dysfunction
* Previous history of blood dyscrasia
* Unable to tolerate the supine position
* Blood donation within the last 3 months
* Recent respiratory tract infection within the past 4 weeks
* Routine medication including aspirin and NSAIDs
18 Years
60 Years
ALL
Yes
Sponsors
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University of Edinburgh
OTHER
Responsible Party
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Principal Investigators
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David E Newby, MD PhD
Role: STUDY_CHAIR
University of Edinburgh
Nicholas L Mills, MBChB PhD
Role: STUDY_DIRECTOR
University of Edinburgh
Amanda L Hunter, MBChB
Role: PRINCIPAL_INVESTIGATOR
University of Edinburgh
Locations
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Royal Infirmary of Edinburgh Clinical Research Facility
Edinburgh, , United Kingdom
Countries
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Other Identifiers
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PG/11/27/28842
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
11-SS-0049
Identifier Type: -
Identifier Source: org_study_id
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