Eligibility Module

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: 2025-12-25 @ 1:46 AM
Ignite Modification Date: 2025-12-25 @ 1:46 AM
NCT ID: NCT05847894
Eligibility Criteria: Inclusion Criteria: * Those aged ≥18 years; or those aged \<18 years who can cooperate with the relevant examination and are accompanied and informed by a guardian; * People with respiratory-related diseases who were to undergo pulmonary examination, or those who volunteered to participate in the trial through publicity recruitment; * expected survival time of 3 months or more; * Those with no previous serious underlying disease and no history of serious eye disease; * Those who can cooperate with ophthalmologic and pulmonary-related examinations and have regular follow-up examinations; * Those who gave informed consent to the study prior to the trial and voluntarily signed the informed consent form; * Other conditions that can be included in the study as judged by the investigator. Exclusion Criteria: * Patients who are unable to complete ophthalmology or pulmonary-related examinations and regular follow-ups due to serious diseases, trauma or surgery (serious ophthalmology diseases such as extremely poor vision that cannot be fixed, ocular atrophy, severe refractive interstitial clouding that prevents fundus photography, etc.); * People with poor compliance due to various reasons such as alcohol or drug dependence, or mental disorders; * Those without informed consent; * Other conditions judged by the investigator to be unsuitable for participation in the trial.
Healthy Volunteers: True
Sex: ALL
Study: NCT05847894
Study Brief:
Protocol Section: NCT05847894