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Clinical Trial Details — Status: Suspended

Administrative data

NCT number NCT00817570
Other study ID # SHEBA-5610-08-IS-CTIL
Secondary ID
Status Suspended
Phase N/A
First received January 4, 2009
Last updated October 21, 2009
Start date April 2009

Study information

Verified date October 2009
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

The purpose of this study is to test and compare the balance reactions of Tranfemoral Amputees and able bodied subjects in response to perturbations given by a highly advanced Virtual Reality system.


Recruitment information / eligibility

Status Suspended
Enrollment 60
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- Transfemoral Amputees, walking without any assistive device, at least one year.

Exclusion Criteria:

- Amputees who suffer from a Neurological Injury/ disease that has implication on balance control.

- Amputees who suffer from Orthopedic Injury that has implication on balance control.

- Amputees who suffer from Cardiology disease that has implication on balance reactions.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Sheba Medical Center Ramat- Gan

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

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