Zinc and Nicotinamide Riboside for Idiopathic Pulmonary Fibrosis
This study is exploring if a clinical trial for idiopathic pulmonary fibrosis (IPF) can successfully recruit and keep participants who complete study tasks from home. Researchers want to see if a combination of zinc and nicotinamide riboside can help treat IPF. You would be compared to others receiving placebos (look-alike substances without active ingredients) to see if these supplements improve symptoms or lung function. The main goal is to learn if it's possible to run this type of study remotely and if participants with IPF might experience better symptoms, quality of life, or daily functioning by taking these supplements. The study is currently unclear on its recruitment status.
- Study design
- This is an interventional study planning to enroll 60 participants. It compares zinc and nicotinamide riboside to matched placebos.
- What's involved
- You would need to be available for the duration of the study and complete study procedures at your local clinical facilities.
- Compensation
- Not stated in the trial record.
- Follow-up
- The study measures feasibility of retention from study activation to 78 weeks.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Zinc and Nicotinamide Riboside for Idiopathic Pulmonary Fibrosis
At a glance
Conditions
NCT06567717
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Cedars-Sinai
Los Angeles, Californiastudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Tanzira Zaman, MD · PRINCIPAL_INVESTIGATOR · Cedars-Sinai
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Feasibility of RetentionFrom study activation to 78 weeks
Feasibility is defined as 80% or more of the enrolled patients complete the 24-week treatment Additional feasibility assessments include the recruitment rate over 52 weeks and the retention rate