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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00353626
Other study ID # SHEBA-06-4211-UG-CTIL
Secondary ID
Status Completed
Phase N/A
First received July 16, 2006
Last updated March 19, 2008
Start date June 2006
Est. completion date September 2007

Study information

Verified date March 2008
Source Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial Summary

Post traumatic amputees with an experience of over 3 months of prosthesis use at home, without any known difficulty using the prosthesis and without stump pathology, using no assistive devices, will be examined in a 3 D computerized gait laboratory. Kinematic and kinetic parameters of gait will be obtained.


Recruitment information / eligibility

Status Completed
Enrollment 9
Est. completion date September 2007
Est. primary completion date July 2007
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 75 Years
Eligibility Inclusion Criteria:

- Post traumatic trans tibial amputees

- No stump pathology

- No assistive devices

- No technical difficulty

Exclusion Criteria:

- Vascular or DM background

- Stump pathology

- Gait difficulties

- Assistive device

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Sheba Medical Center Tel Hashomer

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel,