Efficacy of Steroid Pulse Therapy in Acute Exacerbation of Idiopathic Pulmonary Fibrosis (AE-IPF) Admitted in ER
Primary Purpose
Idiopathic Pulmonary Fibrosis With Acute Exacerbation
Status
Unknown status
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Routine steroid administration group
Steroid pulse therapy group
Sponsored by
About this trial
This is an interventional treatment trial for Idiopathic Pulmonary Fibrosis With Acute Exacerbation
Eligibility Criteria
Inclusion Criteria:
- Among patients with clinically or histologically confirmed idiopathic pulmonary fibrosis, patients who visited the emergency room with dyspnea symptoms
- Patients within 1 month of exacerbation of respiratory symptoms
- Patients with increased GGO or worsening of IPF on chest CT within the last 2 weeks
- Patients who understand the purpose of the clinical study and voluntarily agree to participate in this clinical study
- When it is determined that steroid administration is necessary under the judgment of the medical staff during the treatment process
Exclusion Criteria:
- Patients who complain of dyspnea symptoms due to causes other than the respiratory system, such as fluid overload, congestive heart failure, pulmonary embolism, etc.
- Patients whose respiratory symptoms have worsened for more than 1 month
- Persons who cannot read consent forms (eg. illiterate, foreigners, etc.)
Sites / Locations
- Division of Pulmonology, Department of Internal Medicine, Severance Hospital, Yonsei University College of MedicineRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
Routine
Pulse
Arm Description
Routine steroid administration group
Steroid pulse therapy group
Outcomes
Primary Outcome Measures
mortality rate
mortality rate depending on the steroid dose will be evaluated.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04996303
Brief Title
Efficacy of Steroid Pulse Therapy in Acute Exacerbation of Idiopathic Pulmonary Fibrosis (AE-IPF) Admitted in ER
Official Title
Efficacy of Steroid Pulse Therapy in Acute Exacerbation of Idiopathic Pulmonary Fibrosis (AE-IPF) Admitted in ER
Study Type
Interventional
2. Study Status
Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
July 27, 2021 (Actual)
Primary Completion Date
July 27, 2023 (Anticipated)
Study Completion Date
July 27, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yonsei University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Idiopathic pulmonary fibrosis is the most severe form of interstitial lung disease. It is known that the prognosis is poor due to extensive inflammation and fibrosis of the lung parenchyma. In case of acute exacerbation, the prognosis becomes worse. In early studies, the 3-month mortality rate reached 50-80%, and in a recent study, the 1-month survival rate was 66%, and the 3-month survival rate was 41%.
It is known that 20% of patients with IPF will experience acute exacerbations in their lifetime. The most commonly used treatment for such acute exacerbations is antibiotics and high-dose steroids, or steroid pulse therapy. However, its effectiveness is unclear, and the survival rate is still low. However, as there is no evident therapeutic agent other than steroids, it is included in the treatment guidelines, so conservative treatment is administered while steroids are administered to patients with acute exacerbation of idiopathic pulmonary fibrosis in most upper institutions.
There is no precise treatment other than steroids for patients with idiopathic pulmonary fibrosis-acute exacerbation, but the side effects of steroid administration cannot be overlooked. Therefore, a study is needed to confirm whether steroid pulse therapy is necessary or not.
Inclusion criteria
Among patients with clinically or histologically confirmed idiopathic pulmonary fibrosis, patients who visited the emergency room with dyspnea symptoms
Patients within 1 month of exacerbation of respiratory symptoms
Patients with increased GGO or worsening of IPF on chest CT within the last 2 weeks
Patients who understand the purpose of the clinical study and voluntarily agree to participate in this clinical study
When it is determined that steroid administration is necessary under the judgment of the medical staff during the treatment process
Exclusion criteria
Patients who complain of dyspnea symptoms due to causes other than the respiratory system, such as fluid overload, congestive heart failure, pulmonary embolism, etc.
Patients whose respiratory symptoms have worsened for more than 1 month
Persons who cannot read consent forms (eg. illiterate, foreigners, etc.)
Study design Using an open-label RCT randomization method, the administration will be divided into Group 1 (high-dose followed by low-dose steroid administration) and Group 2 (high-dose/low-dose steroid administration after steroid pulse therapy).
Test group: Group 1 (high dose followed by low dose steroid administration)
Control group: Group 2 (high-dose/low-dose steroid administration after steroid pulse therapy) ▶ Steroid administration Protocol Group 1: Methylprednisolone 1 mg/kg 7 days → 0.5 mg/kg 7 days → 0.25 mg kg 7 days Group 2: Methylprednisolone 10 mg/Kg (500 mg ~ 1g) pulse 3 days -> Methylprednisolone 1 mg/kg 7 days → 0.5 mg/kg 7 days → 0.25 mg/kg 7 days
Response evaluation
The level of inflammatory markers
Imaging improvement: chest x-ray or CT
Pulmonary function test: performed at the outpatient clinic before discharge or 12 weeks after the first visit for acute exacerbation
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Idiopathic Pulmonary Fibrosis With Acute Exacerbation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Routine
Arm Type
Other
Arm Description
Routine steroid administration group
Arm Title
Pulse
Arm Type
Other
Arm Description
Steroid pulse therapy group
Intervention Type
Drug
Intervention Name(s)
Routine steroid administration group
Intervention Description
Steroid administration with routine dose - Methylprednisolone 1 mg/kg 7 days → 0.5 mg/kg 7 days → 0.25 mg kg 7 days
Intervention Type
Device
Intervention Name(s)
Steroid pulse therapy group
Intervention Description
Steroid administration with pulse dose - Methylprednisolone 10 mg/Kg (500 mg ~ 1g) pulse 3 days -> Methylprednisolone 1 mg/kg 7 days → 0.5 mg/kg 7 days → 0.25 mg/kg 7 days
Primary Outcome Measure Information:
Title
mortality rate
Description
mortality rate depending on the steroid dose will be evaluated.
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Among patients with clinically or histologically confirmed idiopathic pulmonary fibrosis, patients who visited the emergency room with dyspnea symptoms
Patients within 1 month of exacerbation of respiratory symptoms
Patients with increased GGO or worsening of IPF on chest CT within the last 2 weeks
Patients who understand the purpose of the clinical study and voluntarily agree to participate in this clinical study
When it is determined that steroid administration is necessary under the judgment of the medical staff during the treatment process
Exclusion Criteria:
Patients who complain of dyspnea symptoms due to causes other than the respiratory system, such as fluid overload, congestive heart failure, pulmonary embolism, etc.
Patients whose respiratory symptoms have worsened for more than 1 month
Persons who cannot read consent forms (eg. illiterate, foreigners, etc.)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Moo Suk Park
Phone
82-2-2228-1954
Email
pms70@yuhs.ac
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Moo Suk Park
Organizational Affiliation
Division of Pulmonology, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Division of Pulmonology, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine
City
Seoul
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Moo Suk Park
Phone
+82-2-2228-1954
Email
pms70@yuhs.ac
12. IPD Sharing Statement
Plan to Share IPD
Undecided
IPD Sharing Plan Description
The IPD could be shared with other researchers, including ILD specialists, especially laboratory data and underlying diseases.
Learn more about this trial
Efficacy of Steroid Pulse Therapy in Acute Exacerbation of Idiopathic Pulmonary Fibrosis (AE-IPF) Admitted in ER
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