Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00815243
Other study ID # 1-2007-2011
Secondary ID
Status Completed
Phase N/A
First received December 26, 2008
Last updated December 26, 2008
Start date September 2007
Est. completion date September 2008

Study information

Verified date December 2008
Source Donetsk National Medical University
Contact n/a
Is FDA regulated No
Health authority Ukraine: Ministry of Health
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether telemedicine consultations (lead by standard scheme)allows to increase quality of anatomical and functional outcomes and improve clinical work-flow at patients with acute bone and joint trauma, hip pathology and congenital orthopedics abnormalities.


Description:

Levels of bad outcomes, untimely death and disability due to acute trauma, specific orthopedic pathology (congenital, coxarthrosis) and non-efficient organisation of clinical work-flow are still very high (especially in rural areas). Standard telemedicine work stations (with special protocols and manuals for original approach to telemedicine activity organisation and management) will be placed into small municipal and rural hospitals. Telemedicine links will be established between 3rd level Trauma&Ortho center and remote sites. Synchronous and asynchronous teleconsultations will be perform for help in evidence-based timely clinical decisions, continual support of clinical wor-flow and treatment process.


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date September 2008
Est. primary completion date April 2008
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Clinical diagnosis of injury of locomotorium (isolated or polytrauma)

- Clinical diagnosis of bone and joint congenital abnormalities or intranatal injury

- Clinical diagnosis of knee, hip arthrosis

- Clinical diagnosis of complication of surgery (unstable, fracture of construction etc)

- Diagnosis is already present

- Primary decision of clinical strategy have to be done (transportation, level of care, method of treatment, surgery peculiarities)

- Indications for teleconsultations determined by physician

Exclusion Criteria:

- Diagnosis is not present

- Patient's self-request for teleconsultations

- No reliable feed-back with attending physician

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Telemedicine consultation
Standard synchronous or asynchronous telemedicine consultations according recommendations and best practice models of ISfTeH
Treatment plan
Treatment plan include diagnostic tests (physical examination, laboratory tests, xray, CT, MRI), medications and surgical treatment (debridements, osteosynthesis, arthroplasty, ORIF etc)

Locations

Country Name City State
Ukraine Central Clinical Municipal Hospital N6 Donetsk
Ukraine Clinics of Maxillo-Fascial Surgery of DNMU Donetsk
Ukraine Donetsk R&D Institute of Traumatology and Orthopedics Donetsk
Ukraine Gorlovka Municipal Hospital N2 Gorlovka Donetskya oblast
Ukraine Volnovakha Central Area Hospital Volnovakha Donetskaya oblast

Sponsors (1)

Lead Sponsor Collaborator
Donetsk National Medical University

Country where clinical trial is conducted

Ukraine, 

References & Publications (2)

Vladzymyrskyy AV. Four years' experience of teleconsultations in daily clinical practice. J Telemed Telecare. 2005;11(6):294-7. — View Citation

Vladzymyrskyy AV. Our experience with telemedicine in traumatology and orthopedics. Ulus Travma Acil Cerrahi Derg. 2004 Jul;10(3):189-91. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Scales for outcomes in trauma and orthopedic (Harris Hip Score, national protocol for trauma outcomes). Sets of criteria: ARR, RRR, AB?, RBI, RR, odds ratio and NNT one year Yes
Secondary "Relevance of Telemedicine Consultation" Questionnaire one year Yes
See also
  Status Clinical Trial Phase
Recruiting NCT04848376 - Post-Market Clinical Follow-up Study of A-SPINE's Products
Terminated NCT03781817 - Intranasal Versus Intravenous Ketamine for Procedural Sedation in Children With Non-operative Fractures Phase 4
Completed NCT04342416 - Using a Brief Visuospatial Interference Intervention to Reduce Intrusive Memories Among Trauma Exposed Women N/A
Recruiting NCT04856449 - DBT Skills Plus EMDR for BPD and Trauma N/A
Completed NCT04356963 - Adjunct VR Pain Management in Acute Brain Injury N/A
Completed NCT05669313 - The Effects of Hypothermia and Acidosis on Coagulation During Treatment With Rivaroxaban Measured With ROTEM
Active, not recruiting NCT03622632 - Pilot Study to Measure Uric Acid in Traumatized Patients: Determinants and Prognostic Association
Recruiting NCT04725721 - Testing FIRST in Youth Outpatient Psychotherapy N/A
Active, not recruiting NCT05530642 - An Augmented Training Program for Preventing Post-Traumatic Stress Injuries Among Diverse Public Safety Personnel N/A
Not yet recruiting NCT05649891 - Checklists Resuscitation Emergency Department N/A
Not yet recruiting NCT03696563 - FreeO2 PreHospital - Automated Oxygen Titration vs Manual Titration According to the BLS-PCS N/A
Withdrawn NCT03249129 - Identification of Autoantibodies and Autoantigens in the Cerebrospinal Fluid of Patients With Spinal Cord Trauma
Completed NCT02240732 - Surgical Tourniquets and Cerebral Emboli N/A
Completed NCT02227979 - Effects of PURPLE Cry Intervention N/A
Withdrawn NCT01169025 - Fentanyl vs. Low-Dose Ketamine for the Relief of Moderate to Severe Pain in Aeromedical Patients N/A
Recruiting NCT01812941 - Evaluation of Mitochondrial Dysfunction in Severe Burn and Trauma Patients N/A
Completed NCT03112304 - Child STEPS for Youth Mental Health in Maine Sustainability N/A
Completed NCT01475344 - Fibrinogen Concentrate (FGTW) in Trauma Patients, Presumed to Bleed (FI in TIC) Phase 1/Phase 2
Completed NCT01210417 - Trauma Heart to Arm Time N/A
Completed NCT01201863 - Neuroendocrine Dysfunction in Traumatic Brain Injury: Effects of Testosterone Therapy Phase 4