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Long-term Oxygen Therapy in Patients With Chronic Obstructive Pulmonary Disease Who Live at High Altitude (COPD-LTOT)

Primary Purpose

COPD

Status
Recruiting
Phase
Not Applicable
Locations
Colombia
Study Type
Interventional
Intervention
Oxygen
Sponsored by
Fundación Neumologica Colombiana
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for COPD focused on measuring Chronic obstructive pulmonary disease, High altitude, Oxygen, long-term oxygen therapy, pulmonary hypertension, chronic hypoxemia

Eligibility Criteria

40 Years - 84 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Men and women between ≥ 40 years and < 85 years living in Bogotá or in a high - altitude city (>2.500 - <3.500 m).
  • Diagnosis of COPD defined by FEV1 / FVC <LLN (Lower limit of normal value) and significant exposure to cigarette ≥ 10 packs / year or woodsmoke ≥ 10 years.
  • Diagnosis of ACO defined by FEV1 / FVC post BD <70%, significant exposure to cigarette or woodsmoke and asthma diagnosed before 40 years and/or wheezing, cough with spirometry with a high respond to bronchodilator (FEV1 or FVC ≥ 15% and 400 ml) or eosinophil >300 cels.
  • PaO2 ≥ 50 and ≤ 55 mmHg or oxygen desaturation during the six-minute walk test (at least in three of the measurements performed during the exam) or during sleep (SpO2 ≤ 85% in ≥ 30% of the total time of sleep)
  • No clinical signs of cor pulmonale
  • Clinically stable COPD defined as no exacerbations in the last three months.
  • Signature of informed consent.

Exclusion Criteria:

  • BMI ≥40.
  • Paraclinical findings of chronic hypoxemia and pulmonary hypertension:

    • Hematocrit ≥ 55%.
    • Pulmonary hypertension (PH) defined by transthoracic echocardiography systolic pulmonary artery pressure > 40 mmHg or indirect signs of PH: Pulmonary artery acceleration time <100ms associated with a meso-systolic notch and flattening of the septum interventricular in systole.
  • Echocardiographic findings that could lead to pulmonary hypertension.

    • Left ventricular systolic dysfunction defined by an ejection fraction <40%
    • Left ventricular diastolic dysfunction higher than grade I.
    • Valvular disease higher than moderate
  • Use of oxygen > 12 hours a day for more than six months in the last year.
  • Comorbidities not controlled or deemed medically that can contribute to mortality during the study follow-up.
  • Diagnosis of severe sleep apnea-hypopnea syndrome without treatment
  • Plan of transfer of residence below 2.500 meters.
  • Medical, psychiatric, social and administrative conditions that define high probability of poor adherence to therapy with oxygen.
  • Active smoking

Sites / Locations

  • Fundación Neumológica ColombianaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Oxygen

Not oxygen

Arm Description

Long-term oxygen therapy in patients with chronic obstructive pulmonary disease (COPD)

No intervention ( no therapy with oxygen)

Outcomes

Primary Outcome Measures

Development of pulmonary hypertension
An echocardiogram will be conducted every ten months to measure the value of pulmonary artery pressure and establish the presence of pulmonary hypertension

Secondary Outcome Measures

Development of polycythemia
A sample of hematocrit and hemoglobine will be perfomed to establish the presence of polycythemia at the begining of the study and every 10 months.
Evaluation of the pulmonary function
Spirometry will be conducted to assess the Forced expiratory volume at 1 second and the Forced vital capacity at the begining of the study and every 10 months.
Number of exacerbations
It will report the number of exacerbations that present the patients during the study
Evaluation of the quality of life
It will perform the St. George Respiratory Questionnaire (SGRQ) to assess the quality of life of the patients at the begining of the study and every 10 months.
Assessment of neurocognitive function
It will make a Mini mental Test to evaluate the neurocognitive performance at the begining of the study and every 10 months.
Evaluation of exercise tolerance
It will conduct a six minute walk test to assess the exercise tolerance at the the begining of the study and every 10 months.

Full Information

First Posted
May 13, 2016
Last Updated
April 4, 2023
Sponsor
Fundación Neumologica Colombiana
Collaborators
Instituto Colombiano para el Desarrollo de la Ciencia y la Tecnología (COLCIENCIAS)
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1. Study Identification

Unique Protocol Identification Number
NCT03020212
Brief Title
Long-term Oxygen Therapy in Patients With Chronic Obstructive Pulmonary Disease Who Live at High Altitude
Acronym
COPD-LTOT
Official Title
Long-term Oxygen Therapy in Patients With Chronic Obstructive Pulmonary Disease (COPD) Who Live at High Altitude (2640 Meters Above Sea Level): Evaluation of a Proposal for Adjusting Criteria
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 2016 (undefined)
Primary Completion Date
November 2023 (Anticipated)
Study Completion Date
January 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fundación Neumologica Colombiana
Collaborators
Instituto Colombiano para el Desarrollo de la Ciencia y la Tecnología (COLCIENCIAS)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
A clinical, prospective, randomized controlled trial to determine the effect of prescribing oxygen in a group of COPD (chronic pulmonary disease) patients with PaO2 (arterial oxygen tension) ≥50 and ≤55 mmHg who do not have erythrocytosis or pulmonary hypertension on echocardiogram (which are considered manifestations of chronic hypoxia)
Detailed Description
A clinical, prospective, randomized controlled trial to determine the effect of prescribing oxygen in a group of COPD patients with PaO2 ≥50 and ≤55 mmHg who do not have erythrocytosis or pulmonary hypertension on echocardiogram (which are considered manifestations of chronic hypoxia). It will be included 220 patients of the Fundación Neumológica Colombiana living in Bogotá who accept their participation by signing an informed consent. The subjects will be randomly assigned to receive or not LTOT and they will be followed for 20 to 30 months. At baseline and then at 10, 20 and 30 months, they will be clinically evaluated with arterial blood gases, pulse oximetry, echocardiography, spirometry with bronchodilator, diffusion capacity, quality of life (SGRQ), neurocognitive performance (MMSE) and six minutes walk test. The primary outcome will evaluate the ratio of occurrence of erythrocytosis or pulmonary hypertension. Secondary outcomes will be evaluated quality of life, lung function, neurocognitive performance and exercise tolerance by comparing the groups with and without LTOT.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COPD
Keywords
Chronic obstructive pulmonary disease, High altitude, Oxygen, long-term oxygen therapy, pulmonary hypertension, chronic hypoxemia

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
220 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Oxygen
Arm Type
Active Comparator
Arm Description
Long-term oxygen therapy in patients with chronic obstructive pulmonary disease (COPD)
Arm Title
Not oxygen
Arm Type
No Intervention
Arm Description
No intervention ( no therapy with oxygen)
Intervention Type
Drug
Intervention Name(s)
Oxygen
Other Intervention Name(s)
LTOT
Intervention Description
The subjects will be randomly assigned to receive or not LTOT and they will be followed for 30 months. At baseline and then at 10, 20 and 30 months, they will be clinically evaluated with arterial blood gases, pulse oximetry, echocardiography, spirometry with bronchodilator, diffusion capacity, quality of life (SGRQ), neurocognitive performance (MMSE) and six minutes walk test. The primary outcome will evaluate the ratio of occurrence of erythrocytosis or pulmonary hypertension. Secondary outcomes will be evaluated quality of life, lung function, neurocognitive performance and exercise tolerance by comparing the groups with and without LTOT.
Primary Outcome Measure Information:
Title
Development of pulmonary hypertension
Description
An echocardiogram will be conducted every ten months to measure the value of pulmonary artery pressure and establish the presence of pulmonary hypertension
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Development of polycythemia
Description
A sample of hematocrit and hemoglobine will be perfomed to establish the presence of polycythemia at the begining of the study and every 10 months.
Time Frame
3 years
Title
Evaluation of the pulmonary function
Description
Spirometry will be conducted to assess the Forced expiratory volume at 1 second and the Forced vital capacity at the begining of the study and every 10 months.
Time Frame
3 years
Title
Number of exacerbations
Description
It will report the number of exacerbations that present the patients during the study
Time Frame
3 years
Title
Evaluation of the quality of life
Description
It will perform the St. George Respiratory Questionnaire (SGRQ) to assess the quality of life of the patients at the begining of the study and every 10 months.
Time Frame
3 years
Title
Assessment of neurocognitive function
Description
It will make a Mini mental Test to evaluate the neurocognitive performance at the begining of the study and every 10 months.
Time Frame
3 years
Title
Evaluation of exercise tolerance
Description
It will conduct a six minute walk test to assess the exercise tolerance at the the begining of the study and every 10 months.
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
84 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women between ≥ 40 years and < 85 years living in Bogotá or in a high - altitude city (>2.500 - <3.500 m). Diagnosis of COPD defined by FEV1 / FVC <LLN (Lower limit of normal value) and significant exposure to cigarette ≥ 10 packs / year or woodsmoke ≥ 10 years. Diagnosis of ACO defined by FEV1 / FVC post BD <70%, significant exposure to cigarette or woodsmoke and asthma diagnosed before 40 years and/or wheezing, cough with spirometry with a high respond to bronchodilator (FEV1 or FVC ≥ 15% and 400 ml) or eosinophil >300 cels. PaO2 ≥ 50 and ≤ 55 mmHg or oxygen desaturation during the six-minute walk test (at least in three of the measurements performed during the exam) or during sleep (SpO2 ≤ 85% in ≥ 30% of the total time of sleep) No clinical signs of cor pulmonale Clinically stable COPD defined as no exacerbations in the last three months. Signature of informed consent. Exclusion Criteria: BMI ≥40. Paraclinical findings of chronic hypoxemia and pulmonary hypertension: Hematocrit ≥ 55%. Pulmonary hypertension (PH) defined by transthoracic echocardiography systolic pulmonary artery pressure > 40 mmHg or indirect signs of PH: Pulmonary artery acceleration time <100ms associated with a meso-systolic notch and flattening of the septum interventricular in systole. Echocardiographic findings that could lead to pulmonary hypertension. Left ventricular systolic dysfunction defined by an ejection fraction <40% Left ventricular diastolic dysfunction higher than grade I. Valvular disease higher than moderate Use of oxygen > 12 hours a day for more than six months in the last year. Comorbidities not controlled or deemed medically that can contribute to mortality during the study follow-up. Diagnosis of severe sleep apnea-hypopnea syndrome without treatment Plan of transfer of residence below 2.500 meters. Medical, psychiatric, social and administrative conditions that define high probability of poor adherence to therapy with oxygen. Active smoking
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Carlos A. Torres-Duque, MD
Phone
( +571) 7428900
Ext
5100
Email
ctorres@neumologica.org
First Name & Middle Initial & Last Name or Official Title & Degree
Mauricio Gonzalez-García, MD
Phone
(+571) 7428900
Ext
5101
Email
mgonzalez@neumologica.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carlos A. Torres-Duque, MD
Organizational Affiliation
Fundación Neumológica Colombiana
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fundación Neumológica Colombiana
City
Bogotá
ZIP/Postal Code
110131
Country
Colombia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carlos A. Torres-Duque, MD
Phone
( +571) 7428900
Ext
5100
Email
ctorres@neumologica.org
First Name & Middle Initial & Last Name & Degree
Mauricio Gonzalez-García, MD
Phone
( +571) 7428900
Ext
5101
Email
mgonzalez@neumologica.org
First Name & Middle Initial & Last Name & Degree
Carlos A. Torres-Duque, MD
First Name & Middle Initial & Last Name & Degree
Mauricio Gonzalez-García, MD
First Name & Middle Initial & Last Name & Degree
Carlos E. Aguirre-Franco, MD
First Name & Middle Initial & Last Name & Degree
Abraham R. Alí-Munive, MD
First Name & Middle Initial & Last Name & Degree
Alejandro Casas-Herrera, MD

12. IPD Sharing Statement

Plan to Share IPD
No
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Long-term Oxygen Therapy in Patients With Chronic Obstructive Pulmonary Disease Who Live at High Altitude

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