Cystic Fibrosis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- The patient must be an infant or child who has been diagnosed with cystic fibrosis (CF) through newborn screening
- The patient must be 18 years old or younger
- Written permission (consent) must be provided by the patient and/or their parent or guardian
Who may not be able to join:
- The patient has needed breathing support (such as a ventilator or oxygen assistance) for more than three days
- The patient has serious birth defects or other significant health conditions beyond cystic fibrosis
- The patient's mother has a history of drug abuse
- The patient's mother has a known serious medical condition
- There are significant difficulties communicating with the patient or their family (confirm with trial site)
- The patient has a pacemaker or wears a continuous glucose monitor (a device that tracks blood sugar levels)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Philipp Latzin, MD PhD, University Children's Hospital Bern
Phone: 0041 31 632 94 93
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Multiple Breath Washout; Spirometry; Body plethysmography; Magnetic Resonance Imaging (MRI); Nasal swabs; Weekly swabs; Swabs during respiratory infection; Routine swabs in CF
Can't join this trial?
Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.