Cost-effectiveness Analysis of Three Corticosteroids in ILDs
Primary Purpose
Interstitial Lung Disease
Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Betamethasone, Dexamethasone, Prednisolone
Sponsored by
About this trial
This is an interventional treatment trial for Interstitial Lung Disease
Eligibility Criteria
Inclusion Criteria:
- Patients with ILD (hypersensitivity pneumonitis) with age between18 and 65 years old.
- Symptoms including dry cough and shortness of breath.
- Significant decrease in pulmonary function (desaturation by 4% after 6-minute walk distance), where the patients were no more controlled on their prednisolone maintenance therapy (up to 10 mg/day).
- Chest CT showing ground glass opacity and band of shadow.
Exclusion Criteria:
- Patients with any other organ affliction (heart failure (ejection fraction 40-50%), renal failure (decrease in glomerular filtration rate > 75%), or liver cirrhosis (transient elastography liver stiffness measurements 12.5-75.5 kPa)).
- Active infection.
- Patients on other immunosuppressive medications (e.g., cyclophosphamide) and anti-fibrotic (e.g., interferon, pirfenidone, endothelin-1 antagonist and tumor necrosis factor α modulator).
- History of pulmonary embolism (corticosteroids' use increase the risk of recurrence of pulmonary embolism).
- Pregnancy.
Sites / Locations
- Faculty of Pharmacy Cairo University
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
Betamethasone group
Dexamethasone group
Prednisolone group
Arm Description
Outcomes
Primary Outcome Measures
Krebs von den Lungen - 6 (KL-6)
a high molecular weight mucin-like glycoprotein expressed on cell surface of alveolar epithelial cells. Elevated levels of KL-6 occur in ILDs and it is recently widely accepted as a biomarker for diagnosis and prognosis of ILDs. Measured as (U/ml) using ELISA
Secondary Outcome Measures
Respiratory Function Assessment; FEV1
FEV1: Forced expiratory volume in the 1st second, measured in (% predicted) using a spirometer
Respiratory Function Assessment; FVC
FVC: Forced Vital Capacity which is the capacity of the lung to air volume, measured in (% predicted) using spirometer.
Respiratory Function Assessment; FEV/FVC Ratio
FEV/FVC: The ratio between the above 2 outcomes
Respiratory Function Assessment; 6MWD
6MWD: the distance walked by the patient after 6 minutes (measured in meters).
Respiratory Function Assessment; % O2 desaturation
% O2 desaturation: the amount of oxygen desaturation that occurs after walking for 6 minutes, measured as the difference between Spo2 before and after the patient walks for 6 minutes (% of oxygen saturation).
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04982809
Brief Title
Cost-effectiveness Analysis of Three Corticosteroids in ILDs
Official Title
Effectiveness and Pharmacoeconomic Study of Using Different Corticosteroids in the Treatment of Interstitial Lung Diseases
Study Type
Interventional
2. Study Status
Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
July 1, 2018 (Actual)
Primary Completion Date
March 15, 2020 (Actual)
Study Completion Date
March 15, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
5. Study Description
Brief Summary
This was a 3 months prospective, open label, and parallel study to test the efficacy of 3 different corticosteroids in the management of interstitial lung diseases. Followed by a pharmacoeconomic analysis to find which regimen (betamethasone, dexamethasone or prednisolone) is the most cost-effective.
Detailed Description
Three different corticosteroid regimens were evaluated for the management of interstitial lung diseases (ILDs) with specific focus on hypersensitivity pneumonitis (HP) where the patients were divided into 3 treatment groups:
Group I: patients receiving weekly pulse doses of betamethasone IM injection (equivalent dose to that of prednisolone daily dose in a week).
Group II: patients receiving weekly pulse doses of dexamethasone IV injection (equivalent dose to that of prednisolone daily dose in a week).
Group III: patients receiving oral prednisolone daily (dose range 15-20 mg/day).
10 mg oral prednisolone oral ≡ 1.5 mg dexamethasone intravenous ≡ 1.2 mg betamethasone intramuscular.
After the administration of the above-mentioned medications, the patients were followed-up over 3 months to evaluate their disease progression. Informed consent was obtained from all subjects or their surrogate after explanation and understanding of the nature, purpose, and potential risks of the study. The study protocol was approved by the Ethics Committee, Faculty of Pharmacy, Cairo University (protocol serial number: CL (2183)) .
A special patient information sheet was designed to collect all information required for data analysis. The sheet was designed to be divided into several sections:
Demographic Data The first section of the patients' information sheet was designed to accommodate the basic general and demographic data (name, address, age, telephone number, social status, weight, and height of the patient). These details were documented from the patient's medical notes.
Medical Data Medical records were used to obtain other data including date and time of examination, the diagnosis, medications on recruitment (if any), smoking habits, patient's medical history, in addition to the patient's medication history.
Parameters Used to Measure Effectiveness as KL-6, PFTs, ESR, CRP
Parameters to Evaluate Treatment Safety Liver Function Tests, Random Blood Glucose (RBG), Blood Pressure
Cost Effectiveness Analysis The study is designed from patient perspective where the direct medical costs as well as the indirect costs (e.g., loss of patients' income) are studied. The costs are collected directly from the patient prospectively throughout the study period. All costs were actual covering the treatment expenses as: the cost of the medications, the cost of administration, the cost of the hospital stay due to ILD during the study period, the cost of the physician's visit and the cost afforded by the patient in order to administer the recommended medication, any extra costs due to exacerbations or adverse effects due to the use of corticosteroids and costs of transportation and days-off.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Interstitial Lung Disease
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
107 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Betamethasone group
Arm Type
Active Comparator
Arm Title
Dexamethasone group
Arm Type
Active Comparator
Arm Title
Prednisolone group
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Betamethasone, Dexamethasone, Prednisolone
Intervention Description
Corticosteroids
Primary Outcome Measure Information:
Title
Krebs von den Lungen - 6 (KL-6)
Description
a high molecular weight mucin-like glycoprotein expressed on cell surface of alveolar epithelial cells. Elevated levels of KL-6 occur in ILDs and it is recently widely accepted as a biomarker for diagnosis and prognosis of ILDs. Measured as (U/ml) using ELISA
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Respiratory Function Assessment; FEV1
Description
FEV1: Forced expiratory volume in the 1st second, measured in (% predicted) using a spirometer
Time Frame
3 months
Title
Respiratory Function Assessment; FVC
Description
FVC: Forced Vital Capacity which is the capacity of the lung to air volume, measured in (% predicted) using spirometer.
Time Frame
3 months
Title
Respiratory Function Assessment; FEV/FVC Ratio
Description
FEV/FVC: The ratio between the above 2 outcomes
Time Frame
3 months
Title
Respiratory Function Assessment; 6MWD
Description
6MWD: the distance walked by the patient after 6 minutes (measured in meters).
Time Frame
3 months
Title
Respiratory Function Assessment; % O2 desaturation
Description
% O2 desaturation: the amount of oxygen desaturation that occurs after walking for 6 minutes, measured as the difference between Spo2 before and after the patient walks for 6 minutes (% of oxygen saturation).
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with ILD (hypersensitivity pneumonitis) with age between18 and 65 years old.
Symptoms including dry cough and shortness of breath.
Significant decrease in pulmonary function (desaturation by 4% after 6-minute walk distance), where the patients were no more controlled on their prednisolone maintenance therapy (up to 10 mg/day).
Chest CT showing ground glass opacity and band of shadow.
Exclusion Criteria:
Patients with any other organ affliction (heart failure (ejection fraction 40-50%), renal failure (decrease in glomerular filtration rate > 75%), or liver cirrhosis (transient elastography liver stiffness measurements 12.5-75.5 kPa)).
Active infection.
Patients on other immunosuppressive medications (e.g., cyclophosphamide) and anti-fibrotic (e.g., interferon, pirfenidone, endothelin-1 antagonist and tumor necrosis factor α modulator).
History of pulmonary embolism (corticosteroids' use increase the risk of recurrence of pulmonary embolism).
Pregnancy.
Facility Information:
Facility Name
Faculty of Pharmacy Cairo University
City
Cairo
ZIP/Postal Code
12411
Country
Egypt
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Cost-effectiveness Analysis of Three Corticosteroids in ILDs
We'll reach out to this number within 24 hrs