Clinical Trials Logo
  1. Home
  2. Wounds and Injuries
  3. NCT01779037
  4. Details
NCT01779037 Clinical Trial

IRF-PAI Functional Outcomes Data(With FIM Instrument Variables)

Wounds and Injuries Clinical Trial

Official title:
IRF-PAI Functional Outcomes Data(With FIM Instrument Variables)

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
See also
  Status Clinical Trial Phase
Recruiting NCT04554212 - Blood Flow Restriction Training After Patellar INStability N/A
Suspended NCT02932176 - Machine Learning for Handheld Vascular Studies
Recruiting NCT04803253 - Study of the Social and Professional Reintegration Improvements Using a Set of Solutions for Upper Limb Amputation N/A
Completed NCT00116337 - Spinal Cord Stimulation to Restore Cough N/A
Completed NCT04438174 - Processed Amniotic Fluid (pAF) for the Treatment of Chronic Wounds Phase 1/Phase 2
Completed NCT03463720 - Outcome for Patients With War-Associated Extremity Wound Infection N/A
Completed NCT03113253 - TRANexamic Acid to Reduce Bleeding in BURN Surgery Phase 4
Not yet recruiting NCT05492903 - COMmunity of Practice And Safety Support for Navigating Pain (COMPASS-NP) N/A
Terminated NCT02909231 - One-year Patient Reported Outcomes Following Hospitalization for Trauma N/A
Completed NCT02432456 - Ketamine Infusion Therapy for the Management of Acute Pain in Adult Rib Fracture Patients Phase 4
Completed NCT02266771 - Impact of V.A.C. Veraflo Therapy in Wounds Requiring Debridement Within an Orthopedic Practice N/A
Completed NCT02744144 - Wound Bacterial Microbiota and Their Antibiotic Resistance N/A
Completed NCT02394821 - Odor Management in Fungating Wounds Comparing Metronidazole and Polihexanide Phase 3
Not yet recruiting NCT01665963 - Efficacy of TopClosure(C)System in Healing Complicated Pacemaker Wounds N/A
Completed NCT00151112 - Comparison of Two Different Procedures for Plexus Anesthesia N/A
Not yet recruiting NCT03872544 - Short Term Status of Free Dermal Fat Autografts for Complex Craniofacial Wounds
Recruiting NCT04596124 - Effectiveness and Tolerability of Fitostimoline Plus Cream and Gauze vs Connettivina Bio Plus Cream and Gauze N/A
Recruiting NCT05800834 - Benefits of Morphine Gel for Pain Reduction in Patients With Cancer Wounds Phase 2
Enrolling by invitation NCT03880188 - Long Term Status of Free Dermal Fat Autografts for Complex Craniofacial Wounds
Terminated NCT04775316 - Prospective, International, Multicenter, Observational Study to Evaluate the Clinical Performance and Safety of a Silicone-coated Transparent Postoperative Dressing

External Links