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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01066923
Other study ID # EMW-2008-FP-01638
Secondary ID
Status Completed
Phase N/A
First received February 5, 2010
Last updated October 10, 2017
Start date February 2010
Est. completion date June 2011

Study information

Verified date October 2017
Source University of Pittsburgh
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if aspirin taken by firefighters prevents platelets from becoming sticky when body temperature rises during work in protective clothing.


Description:

Firefighters have the highest rate of line-of duty death (LODD) in the United States. More than half of these LODD are cardiovascular related occurring disproportionately around fire suppression activities. In addition, shift work, lifestyle factors, and the exposures associated with fire suppression (e.g. smoke, chemicals) may predispose the firefighter to earlier onset of heart disease or cause a pro-inflammatory state leading to endothelial dysfunction.

Fire suppression activities exacerbate cardiovascular strain and endothelial dysfunction and provide potential triggers for ischemic events (e.g. myocardial infarction, stroke). There is a rapid rise in heart rate following the activation of a fire company which may persist for as long as 20 minutes. Even in cases where heavy work is not being performed, the repetitive upper body exercise associated with tool use raises heart rate disproportionately to oxygen consumption.

Finally, there is a rapid rise in core body temperature from increased physical activity, environmental heat and impaired thermoregulation that has been shown to cause vasoconstriction and activate coagulation during heat stress (12, 13). This has recently been demonstrated in firefighters working in thermal protective clothing. The combination of triggers created during fire suppression may result in heart attack or stroke, especially in firefighters with risk factors for cardiovascular disease.

Interventions beyond basic fireground rehab may be required to minimize the effect of these triggers and enhance a firefighter's health and wellness. Fireground rehab typically focuses on cooling and rehydration of the firefighter following fire suppression or training with the assumption that these interventions will correct the underlying pathophysiology. Effective fireground rehab must deliver appropriate interventions and monitor the progress of the firefighter. While correcting hyperthermia and hypohydration are essential for continued performance, it is not clear if these therapies correct alterations in platelet or endothelial function or if other interventions are necessary to correct these physiological disturbances. Furthermore, the options for monitoring the firefighter beyond simply measuring heart and respiratory rate are limited. In our FEMA-funded Fireground Rehab Evaluation (FIRE) Trial, we demonstrated that five commercially available thermometers did not reliably measure or estimate core temperature following uncompensable heat stress (UHS) making it impossible to gauge the effectiveness of rehab interventions.


Recruitment information / eligibility

Status Completed
Enrollment 124
Est. completion date June 2011
Est. primary completion date June 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 49 Years
Eligibility Inclusion Criteria:

1. Apparently healthy males and females aged 18-49 years

Exclusion Criteria:

1. History of heart disease, vascular disease, or sudden death including prior MI, coronary revascularization, congenital heart disease or history of stroke

2. Hypertension during screening: SBP>139 or DBP>89

3. Those who are taking medications that may be expected to blunt the physiologic response to a treadmill exercise test (e.g. beta blockers)

4. Prescription medication with known side effect of impaired thermoregulation

5. Positive pregnancy test at any time during the study

6. Resting ECG with clinical presentation suggesting coronary heart disease (e.g. pathologic Q wave)

7. Known history of gastrointestinal disease or disorder i.e. diverticulitis which creates a theoretical risk of the core temperature capsule becoming lodged in the digestive tract

8. Medications and supplements known to alter endothelial function (e.g. arginine, omega 3 fatty acids, NSAIDS, tobacco products. This exclusion may be disregarded for subjects willing to stop taking the supplement for the duration of the study

9. At the discretion of the study physician for any other medical condition or prescription medication

10. Known history of platelet dysfunction

11. Aspirin allergy or intolerance

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Daily aspirin (ASA)
Two weeks 82 mg aspirin taken orally prior to exercise protocol
Other:
Active cooling
Active cooling to remediate heat stress following exercise by placing hands and forearms into cold water
Drug:
Acute aspirin (ASA)
325 mg chewable aspirin administered immediately following exercise
Other:
Passive cooling
Removing protective garments for passive cooling following exercise
Drug:
Daily placebo
Placebo comparator for daily aspirin therapy
Acute placebo
Placebo comparator for acute aspirin therapy

Locations

Country Name City State
United States University of Pittsburgh, Emergency Responder Human Performance Lab Pittsburgh Pennsylvania

Sponsors (3)

Lead Sponsor Collaborator
Dave Hostler Eyemarker Systems, Inc, Federal Emergency Management Administration

Country where clinical trial is conducted

United States, 

References & Publications (2)

Hostler D, Suyama J, Guyette FX, Moore CG, Pryor RR, Khorana P, McEntire SJ, Comer D, Reis SE. A randomized controlled trial of aspirin and exertional heat stress activation of platelets in firefighters during exertion in thermal protective clothing. Preh — View Citation

Olafiranye O, Hostler D, Winger DG, Wang L, Reis SE. Effect of aspirin on acute changes in peripheral arterial stiffness and endothelial function following exertional heat stress in firefighters: The factorial group results of the Enhanced Firefighter Reh — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Platelet Closure Time 0, 30, 60, and 90 minutes post exercise
Primary Vascular Function Measured by Peripheral Arterial Tonometry Reactive Hyperemia Index Baseline, 30, 60, and 90 minutes post exercise
Secondary Activation of Coagulation This measure was not collected. Equipment was not available. 0, 30, 60, and 90 minutes post exercise
Secondary Hyperthermia and Hemoconcentration Identified by Retinal Imaging This measure was not collected. Equipment was not available. 0, 30, 60, and 90 minutes post exercise
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