Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:15 PM
Ignite Modification Date:
2025-12-24 @ 11:15 PM
NCT ID:
NCT03018756
Eligibility Criteria:
Inclusion Criteria:
* Fibrotic interstitial lung disease (ILD) diagnosis confirmed by specialty ILD clinic
* A total lung capacity (TLC) \<lower limit of normal and ≥60%predicted, a forced vital capacity (FVC) \<lower limit of normal and ≥60%predicted, and a forced expiratory volume in 1 second (FEV1)/FVC \>70%.
* Clinically stable as defined by no changes in medication dosage or frequency of administration with no exacerbations or hospital admissions in the preceding 6 weeks.
* Moderate-to-severe chronic activity related dyspnea as defined by a Baseline Dyspnea Index total score ≤9, modified Medical Research Council score \>1, or oxygen cost diagram.
* Ability to perform all study procedures and provide/sign informed consent.
Exclusion Criteria:
* Women of childbearing age who are pregnant or trying to become pregnant.
* Diffusing capacity of the lung for carbon monoxide (DLCO) \<40 %predicted.
* Presence of active cardiopulmonary disease other than ILD that could contribute to dyspnea and exercise limitation.
* History of allergy or adverse reaction to fentanyl.
* History of allergy or adverse reaction to latex
* Presence of contraindications to pulmonary function or clinical exercise testing, including inability to exercise because of neuromuscular or musculoskeletal disease(s).
* Use of ambulatory oxygen or exercise-induced oxygen desaturation to \< 80% on room air.
* Body mass index (BMI) \<18.5 or ≥35.0 kg/m2.
* Use of antidepressant drugs (i.e., monoamine oxidase inhibitors, serotonin reuptake inhibitors) in the previous 2 weeks.
* Use of opioid drugs (e.g., morphine, fentanyl, oxycodone, codeine, etc.) in the previous 4 weeks.
Note: Healthy volunteers will only be used to assist in the characterization of the IPF study group, i.e., for comparison of baseline exercise responses. They will not undergo treatment.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
40 Years
Study:
NCT03018756
Study Brief:
Protocol Section:
NCT03018756