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Sickness Evaluation at Altitude With Acetazolamide at Relative Doses (SEAWARDII)

Primary Purpose

Acute Mountain Sickness

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Acetazolamide Pill
Sponsored by
Stanford University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Acute Mountain Sickness focused on measuring acetazolamide, chemoprophylaxis, altitude

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Able to complete moderate hike at altitude
  • Live at elevation < 4,000 ft
  • Able to arrange own transportation to study site
  • Available for full study duration (Friday night - Sunday morning)

Exclusion Criteria:

  • Pregnancy
  • Slept at altitude > 4,000 ft within 1 week of study
  • Allergy to acetazolamide or sulfa drugs
  • NSAIDs, acetazolamide, or corticosteroids within 48 hours prior to study start
  • History of severe anemia, severe heart disease, advanced COPD/emphysema or sickle cell disease

Sites / Locations

  • White Mountain Research Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Acetazolamide 125mg twice daily

Acetazolamide 62.5mg twice daily

Arm Description

Acetazolamide pill 125mg twice daily by mouth, started the night prior to ascent and continued for 3 total doses

Acetazolamide pill 62.5mg twice daily by mouth, started the night prior to ascent and continued for 3 total doses

Outcomes

Primary Outcome Measures

Incidence of acute mountain sickness
Incidence of acute mountain sickness by Lake Louise Questionnaire

Secondary Outcome Measures

Full Information

First Posted
January 31, 2019
Last Updated
October 18, 2019
Sponsor
Stanford University
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1. Study Identification

Unique Protocol Identification Number
NCT03828474
Brief Title
Sickness Evaluation at Altitude With Acetazolamide at Relative Doses
Acronym
SEAWARDII
Official Title
Sickness Evaluation at Altitude With Acetazolamide at Relative Doses
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Completed
Study Start Date
August 9, 2019 (Actual)
Primary Completion Date
September 29, 2019 (Actual)
Study Completion Date
September 29, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University

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
Yes

5. Study Description

Brief Summary
The specific aim of this study is to evaluate whether acetazolamide 125mg daily is no worse than acetazolamide 250mg daily in decreasing the incidence of acute mountain sickness (AMS) in travelers to high altitude. The study population is hikers who are ascending at their own rate under their own power in a true hiking environment at the White Mountain Research Station, Owen Valley Lab (OVL) and Bancroft Station (BAR), Bancroft Peak, White Mountain, California
Detailed Description
Acute mountain sickness (AMS) is a constellation of symptoms including headache, sleep disturbance, fatigue, dizziness, and nausea, vomiting, or anorexia that commonly occurs in travelers ascending to altitudes above 2,500m. AMS incidence varies based on altitude and ascent profile with rates reported from 25 to 75% in tourists, trekkers, and mountaineers at North American altitudes. Symptom onset is typically six to twelve hours after arrival at high altitude. This self-limited disease can be debilitating when severe, and left unrecognized or untreated may progress to potentially fatal high altitude cerebral edema (HACE). While gradual ascent has proven effective in preventing AMS, this approach is often impractical to recreationists, search and rescue, disaster relief, and military operations. Acetazolamide increases minute ventilation by 10-20% in subjects at altitude, and hastens acclimatization. It is well established that acetazolamide's main site of action is in the kidney, where it generates a metabolic acidosis through renal bicarbonate wasting and attenuates the effects of hypoxemic-induced respiratory alkalosis. Recommended dosing of acetazolamide for AMS prophylaxis has significantly decreased since early days of use in the 1960s. The current recommended dose of acetazolamide for this indication is 125 mg twice daily, as opposed to historical recommendations of 500mg or 750mg daily. Multiple meta-analyses have concluded that when compared with higher doses, 250mg of acetazolamide daily has been shown to be equally efficacious, with the added benefit of decreasing side effects including paresthesias and dysgeusia. A randomized controlled trial confirmed effectiveness of acetazolamide 125mg twice daily in prevention of AMS when started prior to ascent. In this study, it was found that 125mg twice daily corresponded to a range of 3-5mg/kg/day, depending on subject weight. Within this range, those on the lower dosing range did not have a greater incidence or severity of AMS. For subjects weighing between 50kg (110 lbs) - 83kg (183 lbs), a dose of 250mg/day acetazolamide would fall in this range. Interestingly, mountaineers and trekkers have anecdotally reported protection against AMS with 125mg/day of acetazolamide, a dose below 3-5mg/kg for anyone over 41kg (91lb). Finding the lowest effective dose of acetazolamide for AMS prophylaxis is important because side effects of this medication can mimic AMS, decreasing the specificity of disease scoring on the validated Lake Louise Questionnaire (LLQ) and subsequent AMS diagnosis and chemoprophylactic effectiveness.Keeping in mind that LLQ is scored based on symptoms of headache, gastrointestinal symptoms, fatigue and weakness, and dizziness and lightheadedness, whatever effect acetazolamide has on AMS prevention may be obscured by its side effects that mimic the very same disease. Falsely positive LLQ scores in trekkers and mountaineers taking acetazolamide prophylaxis may lead to unnecessary pharmacologic treatment or even evacuation. From the perspective of high altitude research, participants randomized to or already taking acetazolamide may skew study results by decreasing LLQ specificity and potentially leading researchers to overestimate incidence of AMS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Mountain Sickness
Keywords
acetazolamide, chemoprophylaxis, altitude

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Model Description
Double blind randomized controlled trial
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Visually identical pills
Allocation
Randomized
Enrollment
108 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Acetazolamide 125mg twice daily
Arm Type
Experimental
Arm Description
Acetazolamide pill 125mg twice daily by mouth, started the night prior to ascent and continued for 3 total doses
Arm Title
Acetazolamide 62.5mg twice daily
Arm Type
Experimental
Arm Description
Acetazolamide pill 62.5mg twice daily by mouth, started the night prior to ascent and continued for 3 total doses
Intervention Type
Drug
Intervention Name(s)
Acetazolamide Pill
Other Intervention Name(s)
Diamox
Intervention Description
Acetazolamide pill
Primary Outcome Measure Information:
Title
Incidence of acute mountain sickness
Description
Incidence of acute mountain sickness by Lake Louise Questionnaire
Time Frame
2 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Able to complete moderate hike at altitude Live at elevation < 4,000 ft Able to arrange own transportation to study site Available for full study duration (Friday night - Sunday morning) Exclusion Criteria: Pregnancy Slept at altitude > 4,000 ft within 1 week of study Allergy to acetazolamide or sulfa drugs NSAIDs, acetazolamide, or corticosteroids within 48 hours prior to study start History of severe anemia, severe heart disease, advanced COPD/emphysema or sickle cell disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carrie Jurkiewicz, MD
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
Facility Information:
Facility Name
White Mountain Research Center
City
Bishop
State/Province
California
ZIP/Postal Code
93514
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
19115912
Citation
van Patot MC, Leadbetter G 3rd, Keyes LE, Maakestad KM, Olson S, Hackett PH. Prophylactic low-dose acetazolamide reduces the incidence and severity of acute mountain sickness. High Alt Med Biol. 2008 Winter;9(4):289-93. doi: 10.1089/ham.2008.1029.
Results Reference
background
PubMed Identifier
17023566
Citation
Leaf DE, Goldfarb DS. Mechanisms of action of acetazolamide in the prophylaxis and treatment of acute mountain sickness. J Appl Physiol (1985). 2007 Apr;102(4):1313-22. doi: 10.1152/japplphysiol.01572.2005. Epub 2006 Oct 5.
Results Reference
background
PubMed Identifier
11450659
Citation
Hackett PH, Roach RC. High-altitude illness. N Engl J Med. 2001 Jul 12;345(2):107-14. doi: 10.1056/NEJM200107123450206. No abstract available.
Results Reference
background
PubMed Identifier
32479750
Citation
Lipman GS, Jurkiewicz C, Burnier A, Marvel J, Phillips C, Lowry C, Hawkins J, Navlyt A, Swenson ER. A Randomized Controlled Trial of the Lowest Effective Dose of Acetazolamide for Acute Mountain Sickness Prevention. Am J Med. 2020 Dec;133(12):e706-e715. doi: 10.1016/j.amjmed.2020.05.003. Epub 2020 May 29.
Results Reference
derived

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Sickness Evaluation at Altitude With Acetazolamide at Relative Doses

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