Status:
COMPLETED
Feasibility Study Focusing on Fit of Made-to-measure Compression Garments in Healthy Subjects II
Lead Sponsor:
BSN Medical GmbH
Collaborating Sponsors:
proDERM GmbH
Conditions:
Product Use Issue
Eligibility:
All Genders
18-70 years
Phase:
NA
Brief Summary
Fit of made-to-measure compression garments in healthy subjects will be tested on one day, simulating daily activities.
Detailed Description
Lower extremities of 36 healthy subjects will be measured by trained experts to collect measures for made-to-measure compression garments. Fit of made-to-measure compression garments, which are not o...
Eligibility Criteria
Inclusion
- Men, women or diverse
- Full legal competence
- Age between 18 and 70 years
- Capability to understand the subject information and to provide conscious informed consent
- All female or diverse subjects of childbearing potential must either be surgically sterile (hysterectomy or tubal ligation) or agree to use a reliable method of contraception with a failure rate of a Pearl-Index less than 1% per year when used consistently and correctly such as implants, injectables, combined oral contraceptives, some intra uterine devices, sexual abstinence or vasectomized partner for at least 4 weeks
- Willingness to conduct a urine pregnancy test for all female or diverse subjects of childbearing potential
- Capability and willingness to follow protocol requirements
- Signed informed consent for study participation and data protection regulations
- BMI \>23 kg/m² and ≤ 40 kg/m²
Exclusion
- Circumference of the largest circumference of the upper leg \>90 cm (measured in the upright position)
- Shape distortions between the waist and the feet
- Diagnosed lymphedema of the lower extremities
- Diagnosed lipedema of lower extremities
- Diagnosed indication for therapy with flat-knitted compression garments
- Alcohol abuse as reported by subject and/ or suspected by investigator
- Drug abuse as reported by subject and/ or suspected by investigator
- Allergy or sensitivity to one or more components of the investigational devices, as far as reported by the subject
- Pregnancy or breastfeeding
- Diagnosed peripheral arterial disease
- Presence of untreated phlebitis, or septic phlebitis
- Diagnosed progressed arterial insufficiency including ischemia
- Diagnosed congestive heart failure
- Diagnosed clinically relevant hypertension
- Diagnosed renal insufficiency or kidney failure
- Presence of Untreated or progressing skin infection
- Presence of large coagulum in the leg vein
- Presence of phlegmasia coerulea dolens
- Diagnosed Raynaud's disease
- Diagnosed gonarthrosis
- Diagnosed ankle arthrosis
- Diagnosed rheumatoid arthritis
- Presence of exuding dermatoses
- Presence of gangrene
- Diagnosed malign lymphedema
- Diagnosed psoriasis
- Diagnosed diabetes mellitus
- Diagnosed complex regional pain syndrome (CRPS; Sudeck atrophy)
- Diagnosed polyneuropathy
- Diagnosed severe impaired skin sensitivity und impaired sensitivity of the extremities, including all sensory malfunctions and diagnosed impaired pain sensitivity
- Objections of the investigator to the subject's participation in the trial due to medical reasons or any other reason for which the subject should not participate in the opinion of the investigator
- Participation in any clinical investigation with systemic and/or pharmaceutical substances within the last 4 weeks and/or in parallel
- Sponsors, manufacturers or CRO staff
- Surgery in the test area within the last 4 weeks
- Open wounds in the test area
Key Trial Info
Start Date :
February 23 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 12 2021
Estimated Enrollment :
36 Patients enrolled
Trial Details
Trial ID
NCT04714476
Start Date
February 23 2021
End Date
March 12 2021
Last Update
February 5 2025
Active Locations (1)
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1
proDERM GmbH Institut für Angewandte Dermatologische Forschung
Schenefeld, Schleswig-Holstein, Germany, 22869