NL-OMON45575CompletedNot Applicable
Clinical usability of non-contact scanners in measuring stumpvolume of transtibial amputee patients - CCUNCMSTAP
Isala Klinieken0 sites36 target enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 36
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 18 to 64 (—)
Inclusion Criteria
- •Uni- or bilateral transtibial amputation
- •Operation of the stump more than 1 year ago
- •Older than 18 years
- •Informed consent
- •Availability at research data
Exclusion Criteria
- •Less than 1 year ago an operation of the stump
- •Large changes in stump volume during the day with co-morbidity like heart failure, kidney failure, deep vein thrombosis, lymphedema, fracture of the leg, rheumatoid artritis, CRPS, dermatologic diseases associated with edema.
- •Wound at the stump of more than 1 cm amplitude and/or signs of infection, in which clinically may be assumed that this will influence the stumpvolume
- •Weakness of upperleg which causes inability to lift the leg up in the air
- •Not able to make a transfer from (wheel)chair to research table
- •Not enough understanding of the Dutch language to give answer to simple questions, follow simple instructions or understand the informed consent letter
Investigators
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