Sildenafil for Swimming-Induced Pulmonary Edema (SIPE) Prevention
Primary Purpose
Edema, Pulmonary, Immersion, Diving
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Sildenafil Citrate
Placebo Oral Tablet
Sponsored by
About this trial
This is an interventional prevention trial for Edema, Pulmonary
Eligibility 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)
Sites / Locations
- Duke University Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
Placebo
Sildenafil
Arm Description
Each participant will be studied with active drug and placebo.
Sildenafil 50 mg orally one hour (once) before immersed exercise
Outcomes
Primary Outcome Measures
Number of Participants With Pulmonary Edema
One or more of: hypoxemia, productive cough, pulmonary edema on chest radiograph, wheezing on chest auscultation.
Secondary Outcome Measures
Number of Participants With Dyspnea Leading to Voluntary Premature Cessation of Exercise
Voluntary premature cessation of exercise due to shortness of breath.
Number of Participants With Post-exercise 10% Decrease in Forced Vital Capacity (FVC) or Forced Expiratory Volume in One Second (FEV1) as Measured by Spirometry
Post-exercise 10% decrease in forced vital capacity (FVC) or forced expiratory volume in one second (FEV1).
Number of Participants With "Comet Tails" Seen on Ultrasound of the Lungs
A "comet tail" artefact is a short path reverberation artefact that weakens with each reverberation, resulting in a vertical echogenic artefact that rapidly fades as it continues in to the ultrasound image.
Number of Participants Who Found the Exercise Easiest When Given Sildenafil Citrate Versus When Given Placebo
Full Information
NCT ID
NCT03686813
First Posted
September 24, 2018
Last Updated
October 28, 2022
Sponsor
Duke University
Collaborators
United States Department of Defense
1. Study Identification
Unique Protocol Identification Number
NCT03686813
Brief Title
Sildenafil for Swimming-Induced Pulmonary Edema (SIPE) Prevention
Official Title
Sildenafil for Prevention of Swimming-Induced Pulmonary Edema (SIPE)
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
July 15, 2019 (Actual)
Primary Completion Date
October 29, 2021 (Actual)
Study Completion Date
October 29, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duke University
Collaborators
United States Department of Defense
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No
5. 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.
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Edema, Pulmonary, Immersion, Diving
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Model Description
Double blind, randomized
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Placebo controlled
Allocation
Randomized
Enrollment
18 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Each participant will be studied with active drug and placebo.
Arm Title
Sildenafil
Arm Type
Active Comparator
Arm Description
Sildenafil 50 mg orally one hour (once) before immersed exercise
Intervention Type
Drug
Intervention Name(s)
Sildenafil Citrate
Other Intervention Name(s)
Viagra, Revatio
Intervention Description
Oral sildenafil, 50 mg
Intervention Type
Drug
Intervention Name(s)
Placebo Oral Tablet
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Number of Participants With Pulmonary Edema
Description
One or more of: hypoxemia, productive cough, pulmonary edema on chest radiograph, wheezing on chest auscultation.
Time Frame
During or immediately after exercise in cold water, approximately one hour and 40 minutes
Secondary Outcome Measure Information:
Title
Number of Participants With Dyspnea Leading to Voluntary Premature Cessation of Exercise
Description
Voluntary premature cessation of exercise due to shortness of breath.
Time Frame
During or immediately after exercise in cold water, approximately one hour and 40 minutes
Title
Number of Participants With Post-exercise 10% Decrease in Forced Vital Capacity (FVC) or Forced Expiratory Volume in One Second (FEV1) as Measured by Spirometry
Description
Post-exercise 10% decrease in forced vital capacity (FVC) or forced expiratory volume in one second (FEV1).
Time Frame
Immediately after exercise in cold water, approximately one hour and 40 minutes
Title
Number of Participants With "Comet Tails" Seen on Ultrasound of the Lungs
Description
A "comet tail" artefact is a short path reverberation artefact that weakens with each reverberation, resulting in a vertical echogenic artefact that rapidly fades as it continues in to the ultrasound image.
Time Frame
Immediately after exercise in cold water, approximately one hour and 40 minutes
Title
Number of Participants Who Found the Exercise Easiest When Given Sildenafil Citrate Versus When Given Placebo
Time Frame
Immediately after exercise in cold water, approximately one hour and 40 minutes
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility 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)
Facility Information:
Facility Name
Duke University Medical Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
IPD Sharing Plan Description
Data will be published in the open literature
Learn more about this trial
Sildenafil for Swimming-Induced Pulmonary Edema (SIPE) Prevention
We'll reach out to this number within 24 hrs