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Clinical Trials/NL-OMON45575
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

Sponsor
Isala Klinieken

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