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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01779037
Other study ID # IRFPAIdata
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date January 2001
Est. completion date May 1, 2018

Study information

Verified date May 2018
Source Uniform Data System for Medical Rehabilitation
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

IRF-PAI Functional Outcomes Data, including FIM instrument variables


Description:

United States IRF functional outcomes, medical and socio-demographic data for years 2002-2015


Recruitment information / eligibility

Status Terminated
Enrollment 0
Est. completion date May 1, 2018
Est. primary completion date May 1, 2018
Accepts healthy volunteers No
Gender All
Age group 7 Years to 100 Years
Eligibility Inclusion Criteria:

- Admission to an inpatient rehabilitation facility

Exclusion Criteria:

- Admission to acute, SNF setting, etc.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States UDSMR Buffalo New York

Sponsors (1)

Lead Sponsor Collaborator
Uniform Data System for Medical Rehabilitation

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary IRF-PAI Assessment Instrument(including the FIM instrument) admission/discharge
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