Structured Discharge and Follow-up Protocol for COPD Patients Receiving LTOT and NIV

NCT03499470 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 160

Last updated 2019-07-18

No results posted yet for this study

Summary

Readmission to hospital is one of the most important problems in chronic obstructive pulmonary disease (COPD) patients who developed chronic respiratory failure. Patients receiving long-term oxygen therapy (LTOT) and noninvasive ventilation (NIV) constitute the most vulnerable group because of the need for comprehensive care. However, because of lack of health care support systems in Turkey, many advanced COPD patients are hospitalized due to preventable problems such as insufficient knowledge about the therapies, nonadherence to therapy and technical issues related to LTOT/NIV equipment. The aim of this multicenter randomized trial is to find out whether a structured discharge and follow-up protocol reduce the rate of unplanned, COPD-related hospital readmissions over 90 days in patients receiving LTOT or NIV.

Conditions

  • COPD Exacerbation
  • Noninvasive Ventilation
  • Long Term Oxygen Therapy
  • Chronic Respiratory Failure

Interventions

OTHER

Protocol for structured discharge and follow-up

Sponsors & Collaborators

  • Celal Bayar University

    collaborator OTHER
  • Ege University

    collaborator OTHER
  • Gazi University

    collaborator OTHER
  • Duzce University

    collaborator OTHER
  • Cukurova University

    collaborator OTHER
  • Ataturk University

    collaborator OTHER
  • Uludag University

    collaborator OTHER
  • Atatürk Chest Diseases and Chest Surgery Training and Research Hospital

    collaborator OTHER
  • Istanbul Sureyyapasa Chest Diseases and Chest Surgery Training and Research Hospital

    collaborator OTHER
  • T.C. ORDU ÜNİVERSİTESİ

    collaborator OTHER
  • Hacettepe University

    collaborator OTHER
  • Turkish Directorate General of Public Health

    collaborator UNKNOWN
  • Istanbul University - Cerrahpasa

    collaborator OTHER
  • Diskapi Yildirim Beyazit Education and Research Hospital

    collaborator OTHER_GOV
  • Dokuz Eylul University

    lead OTHER

Principal Investigators

  • BEGUM ERGAN, MD · Dokuz Eylul University

  • TUGBA GOKTALAY, MD · Celal Bayar University

  • PINAR ERGUN, MD · Health Sciences University Ataturk Chest Diseases and Chest Surgery Hospital

  • ALEV GURGUN, MD · Ege University

  • METIN AKGUN, MD · Ataturk University

  • NURDAN KOKTURK, MD · Gazi University

  • EZGI OZYILMAZ, MD · Cukurova University

  • ASLI DILEKTASLI, MD · Uludag University

  • BIRSEN OCAKLI, MD · Health Sciences University Sureyyapasa Chest Diseases and Chest Surgery Hospital

  • ONER BALBAY, MD · Duzce University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-11-07
Primary Completion
2019-08-31
Completion
2019-08-31

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03499470 on ClinicalTrials.gov