Burned skin areas, which were initially vital, can be irreversibly damaged by wound
progression. The aim of the present study is to evaluate the feasibility of ischemic
conditioning to reduce secondary wound progression.
Procedure: Remote ischemic conditioning
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Full eligibility criteria for NCT03027596
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Ability to understand the study information and the consent to sign
Thermal injury (burn / scalding) with a clinical evaluated depth of at least 2a
At least one of the following sites must not have skin lesions
: Upper arm right and left
hospital admission within 6 hours after trauma has taken place
Participation in another experimental study
Pregnancy (women are subjected to a pregnancy test (urine)
Contraindication for the use of the tourniquet, for example Lymph drainage disorders after axillary lymphadenectomy or Irradiation of the axilla
Non-compliant patients who are, e.g. Intubated
Pure 3rd degree burns (full thickness) or charring
Thermal injuries older than 6 hours
All locations for NCT03027596
BG Trauma Center, University Tübingen, Germany
Tuebingen, Germany, 72076
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View full eligibility
Tris trial is registered with FDA with number: NCT03027596. The sponsor of the trial is BG Trauma Center Tuebingen and it is looking for 140 volunteers for the current phase.
Official trial title: Remote Ischemic Conditioning to Reduce Burn Wound Progression
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