Sildenafil for Swimming-Induced Pulmonary Edema (SIPE) Prevention
Study Details
Study Description
Brief Summary
This trial is testing the effectiveness of a single oral dose of sildenafil (50 mg) taken 1 hour before a provocative event on the subsequent development of swimming-induced pulmonary edema.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Detailed Description
Immersion pulmonary edema (also known as swimming-induced pulmonary edema, SIPE) is a condition in which the lungs fill with fluid (pulmonary edema) during a dive or vigorous swim, causing cough with bloody sputum, shortness of breath and reduced blood oxygen levels. In the Navy this usually occurs in young, healthy individuals such as SEAL and Special Warfare Combatant-Craft trainees. SIPE generally resolves spontaneously within 24 hours but it can be fatal. It is believed that SIPE is responsible for some deaths in civilians during triathlons. This proposal aims to test a drug to prevent SIPE.
Depending upon severity, the prevalence of SIPE is reported in up to 60% during 2.4-3.6 km open sea swimming trials in the Israel Defense Force. In SEAL training in the US approximately 40 cases per year (around 3%) have been reported, more commonly during winter, when it is observed in up to 5% of trainees. Return to duty time can be up to 7 days. SIPE also affects other groups of highly fit individuals such as triathletes. In susceptible individuals it tends to recur, thus a preventive medicine would be useful for both Navy SEALs and civilians.
The aim of this study will be to provide the Navy an FDA-approved drug that can be used to prevent SIPE. The investigators hypothesize that sildenafil administration to SIPE-susceptible individuals one hour before a swim in cold water will reduce or eliminate the risk of SIPE. The method to be used to test this hypothesis will be a 40-minute period of exercise immersed to the neck in 20°C water, a test that results in SIPE symptoms in the majority of susceptible individuals. The investigators plan to study 20 individuals who have previously experienced SIPE. Each volunteer will be tested twice. Either sildenafil or an inactive drug (placebo) administered in random order will be given prior to each exercise. For each participant exercise periods will be performed at least 7 days apart. The identity of the drug and placebo will be concealed from the investigators and the volunteers until the end of the study. The number of instances in which SIPE manifestations after sildenafil and placebo will then be compared.
Availability of a drug that can prevent SIPE would provide the Navy with a useful tool that could be administered to SEALs who have experienced SIPE prior to critical missions. It would also be useful for civilians who have experienced SIPE but wish to continue with the precipitating exercise such as swimming or competing in triathlons, and also for patients with heart failure for whom swimming induces shortness of breath or pulmonary edema.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Placebo Comparator: Placebo Each participant will be studied with active drug and placebo. |
Drug: Placebo Oral Tablet
Placebo
|
| Active Comparator: Sildenafil Sildenafil 50 mg orally one hour (once) before immersed exercise |
Drug: Sildenafil Citrate
Oral sildenafil, 50 mg
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Pulmonary edema [During or immediately after exercise in cold water]
One or more of: hypoxemia, productive cough, pulmonary edema on chest radiograph, wheezing on chest auscultation
Secondary Outcome Measures
- Dyspnea [During or immediately after exercise in cold water]
Voluntary premature cessation of exercise due to shortness of breath
- Spirometry [Immediately after exercise in cold water]
Post-exercise 10% decrease in forced vital capacity (FVC) or forced expiratory volume in one second (FEV1)
- Ultrasound lung assessment [Immediately after exercise in cold water]
'Comet tails' seen on ultrasound of the lungs
- Ease of exercise completion [Immediately after exercise in cold water]
Subjective ease with which exercise was completed
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Healthy volunteers between 18 and 45 years
-
History of swimming-induced pulmonary edema
Exclusion Criteria:
-
Pregnant women
-
Significant heart valve disease
-
Cardiomyopathy
-
Uncontrolled hypertension
-
Coronary artery disease
-
Obstructive lung disease
-
VO2max <25 mL/kg as estimated by the University of Houston Non-Exercise Test
-
Previous adverse reaction to sildenafil
-
Use of antihypertensives or other drugs that are known to interact adversely with sildenafil (e.g. nitrates, alpha adrenergic blockers)
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Duke University Medical Center | Durham | North Carolina | United States | 27710 |
Sponsors and Collaborators
- Duke University
- United States Department of Defense
Investigators
None specified.Study Documents (Full-Text)
More Information
Publications
None provided.- Pro00100971