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Blister Eradication Looking at Impact of Experimental Versus Established Regimens (BELIEVER)

Primary Purpose

Blister of Foot

Status
Unknown status
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Elastikon
Rocktape
Sponsored by
Stanford University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Blister of Foot

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • The study enrollment period will run for approximately 7 days over 3 weeks throughout 2019 at Racing the Planet races in Namibia, Mongolia and Chile. All racers are potential subjects.

Subjects will be enrolled when they present to the medical tent for the treatment of their first painful blister. The subject will be evaluated for exclusion criteria and the subject will be asked to select the most painful blister to be included in the study. All other blisters may be treated through traditional means and are not included in the study.

Exclusion Criteria:

  • Blister exclusion criteria:

    1. Toe blisters will be excluded because they are treated with paper tape only to avoid friction against neighboring toes and further blister formation.
    2. Only intact blisters are included in this study as de-roofed blisters are treated differently.
    3. Hemorrhagic blisters are excluded as they are often not amenable to percutaneous drainage given the increased risk in infection.

If the most painful blister is a toe blister or a hemorrhagic blister, then the second most painful blister will be selected. If there is no second blister, the subject cannot be enrolled at this time.

Sites / Locations

  • Racing the PlanetRecruiting
  • Racing the PlanetRecruiting
  • Namib DesertRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Elastikon - traditional

Rocktape - novel

Arm Description

The participant will be randomized to a treatment arm according to their racing bib number. Even bib numbers will be in the Elastikon treatment arm. The researcher will evaluate the blister and treat according to treatment arm with the following blister treatment device intervention: the blister will be prepped per routine, drained, covered with paper tape, sprayed with adhesive spray and then covered with Elastikon.

The participant will be randomized to a treatment arm according to their racing bib number. Odd bib numbers will be in the Rocktape treatment arm. The researcher will evaluate the blister and treat according to treatment arm with the following blister treatment device intervention: the blister will be prepped per routine, drained, covered with paper tape and then covered with Rocktape

Outcomes

Primary Outcome Measures

Treatment success
The subject's involvement in the study will end in one of the following situations and the researcher will fill out the appropriate data sheet at the time of the subject's departure from the study. The blister treatment is a success as defined by: the blister treatment falls off and the subject has no pain and no blister reoccurrence the blister treatment is removed by the subject and does not need to be replaced because the there is no pain or blister present the blister treatment stays on for the length of the study needing no intervention The blister treatment is a failure as defined by: if the blister re-occurs if the treated area has pain to the point that the blister treatment must be removed to evaluate if the subject removes the blister treatment and needs to be retreated. The race has come to completion The subject withdraws from the race or the study.

Secondary Outcome Measures

Full Information

First Posted
February 2, 2019
Last Updated
June 22, 2021
Sponsor
Stanford University
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1. Study Identification

Unique Protocol Identification Number
NCT03835806
Brief Title
Blister Eradication Looking at Impact of Experimental Versus Established Regimens
Acronym
BELIEVER
Official Title
Blister Eradication Looking at Impact of Experimental Versus Established Regimens
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Unknown status
Study Start Date
April 27, 2019 (Actual)
Primary Completion Date
August 31, 2022 (Anticipated)
Study Completion Date
August 31, 2022 (Anticipated)

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
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The specific aim of this study is to evaluate whether RockTape has similar efficacy to Elastikon in the treatment of foot blisters in ultramarathon runners. Elastikon with paper tape and spray adhesive is a well-accepted means of blister treatment and has been used by medical staff at over 50 multi-stage ultramarathons around the world. RockTape is another commercially available product that has also been used by runners successfully to treat foot blisters. RockTape's adhesive qualities have a potential advantage over Elastikon, in that it does not require an additional adhesive substituting a level of complexity, weight, and cost for foot care. There have been no studies examining the efficacy of either agent for blister treatment. This randomized controlled trial will compare the traditional method of treating blisters with a multi-step approach of percutaneous drainage, paper tape, spray adhesive and then Elastikon to percutaneous drainage, paper tape and RockTape.
Detailed Description
Friction foot blisters are one of the most common injuries encountered by hikers and runners(1) with incidence as high as 39% in marathoners(2). In adventure races it is the most commonly reported injury(3) and in expedition length ultramarathons, blisters account for nearly 74% of medical visits(4). While most blisters are of minor medical significance, they can impair concentration, decrease athletic performance, and can be potentially debilitating. The specific aim of this study is to evaluate whether RockTape has similar efficacy to Elastikon in the treatment of foot blisters in ultramarathon runners. Elastikon with paper tape and spray adhesive is a well-accepted means of blister treatment and has been used by medical staff at over 50 multi-stage ultramarathons around the world. RockTape is another commercially available product that has also been used by runners successfully to treat foot blisters. RockTape's adhesive qualities have a potential advantage over Elastikon, in that it does not require an additional adhesive substituting a level of complexity, weight, and cost for foot care. There have been no studies examining the efficacy of either agent for blister treatment. This randomized controlled trial will compare the traditional method of treating blisters with a multi-step approach of percutaneous drainage, paper tape, spray adhesive and then Elastikon to percutaneous drainage, paper tape and RockTape.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Blister of Foot

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This is a randomized control trial looking at a novel blister treatment intervention versus a traditional model.
Masking
None (Open Label)
Masking Description
The treatments are visually dissimilar, therefore blinding for the investigator and subject is not possible.
Allocation
Randomized
Enrollment
130 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Elastikon - traditional
Arm Type
Active Comparator
Arm Description
The participant will be randomized to a treatment arm according to their racing bib number. Even bib numbers will be in the Elastikon treatment arm. The researcher will evaluate the blister and treat according to treatment arm with the following blister treatment device intervention: the blister will be prepped per routine, drained, covered with paper tape, sprayed with adhesive spray and then covered with Elastikon.
Arm Title
Rocktape - novel
Arm Type
Experimental
Arm Description
The participant will be randomized to a treatment arm according to their racing bib number. Odd bib numbers will be in the Rocktape treatment arm. The researcher will evaluate the blister and treat according to treatment arm with the following blister treatment device intervention: the blister will be prepped per routine, drained, covered with paper tape and then covered with Rocktape
Intervention Type
Other
Intervention Name(s)
Elastikon
Intervention Description
This randomized controlled trial will compare the traditional method of treating blisters with a multi-step approach of percutaneous drainage, paper tape, spray adhesive and then Elastikon which is our traditional blister treatment approach.
Intervention Type
Other
Intervention Name(s)
Rocktape
Intervention Description
This randomized controlled trial will compare the traditional method of treating blisters with a multi-step approach of percutaneous drainage, paper tape and then Rocktape which is our novel blister treatment approach.
Primary Outcome Measure Information:
Title
Treatment success
Description
The subject's involvement in the study will end in one of the following situations and the researcher will fill out the appropriate data sheet at the time of the subject's departure from the study. The blister treatment is a success as defined by: the blister treatment falls off and the subject has no pain and no blister reoccurrence the blister treatment is removed by the subject and does not need to be replaced because the there is no pain or blister present the blister treatment stays on for the length of the study needing no intervention The blister treatment is a failure as defined by: if the blister re-occurs if the treated area has pain to the point that the blister treatment must be removed to evaluate if the subject removes the blister treatment and needs to be retreated. The race has come to completion The subject withdraws from the race or the study.
Time Frame
Data will be collected during the 1 week ultramarathon in austere conditions until study completion, usually 3-5 days. This will be conducted over 3 separate races.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: The study enrollment period will run for approximately 7 days over 3 weeks throughout 2019 at Racing the Planet races in Namibia, Mongolia and Chile. All racers are potential subjects. Subjects will be enrolled when they present to the medical tent for the treatment of their first painful blister. The subject will be evaluated for exclusion criteria and the subject will be asked to select the most painful blister to be included in the study. All other blisters may be treated through traditional means and are not included in the study. Exclusion Criteria: Blister exclusion criteria: Toe blisters will be excluded because they are treated with paper tape only to avoid friction against neighboring toes and further blister formation. Only intact blisters are included in this study as de-roofed blisters are treated differently. Hemorrhagic blisters are excluded as they are often not amenable to percutaneous drainage given the increased risk in infection. If the most painful blister is a toe blister or a hemorrhagic blister, then the second most painful blister will be selected. If there is no second blister, the subject cannot be enrolled at this time.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Patrick B Burns, MD
Phone
9788663533
Email
pburns@stanford.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Grant Lipman, MD
Phone
4152909286
Email
gslipman@stanford.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patrick B Burns, MD
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Racing the Planet
City
San Pedro de Atacama
Country
Chile
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Patrick B Burns, MD
Phone
9788663533
Email
pburns@stanford.edu
Facility Name
Racing the Planet
City
Ulaan Baatar
Country
Mongolia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Patrick B Burns, MD
Phone
9788663533
Email
pburns@stanford.edu
Facility Name
Namib Desert
City
Windhoek
Country
Namibia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Patrick B Burns, MD
Phone
9788663533
Email
pburns@stanford.edu

12. IPD Sharing Statement

Plan to Share IPD
No

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Blister Eradication Looking at Impact of Experimental Versus Established Regimens

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