Prospective Study of Pregnancy in Women With Cystic Fibrosis (NCT04828382)

Check every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).

1. Pregnant, intending to continue pregnancy, enrolled in the Cystic Fibrosis Foundation Patient Registry (CFFPR)

🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.

📍 All Participating Trial Locations (40 Sites)

Showing the first 25 of 40 sites.

• University of Alabama at Birmingham — Birmingham, Alabama
• University of Arkansas for Medical Sciences — Little Rock, Arkansas
• University of California San Diego — La Jolla, California
• National Jewish Health — Denver, Colorado
• University of Florida — Gainesville, Florida
• Joe DiMaggio Children's Hospital — Hollywood, Florida
• Emory University — Atlanta, Georgia
• Saint Luke's Cystic Fibrosis Center of Idaho — Boise, Idaho
• Indiana University Medical Center — Indianapolis, Indiana
• University of Kansas Medical Center — Kansas City, Kansas
• University of Kentucky — Lexington, Kentucky
• Tulane University — New Orleans, Louisiana
• John Hopkins Hospital — Baltimore, Maryland
• Massachusetts General Hospital — Boston, Massachusetts
• Boston Children's Hospital, Brigham & Women's Hospital — Boston, Massachusetts
• University of Michigan Health System — Ann Arbor, Michigan
• Helen DeVos Children's Hospital — Grand Rapids, Michigan
• The Minnesota Cystic Fibrosis Center — Minneapolis, Minnesota
• Washington University School of Medicine — St Louis, Missouri
• University of Nebraska Medical Center — Omaha, Nebraska
• The Cystic Fibrosis Center of Western New York — Buffalo, New York
• Columbia University Cystic Fibrosis Program — New York, New York
• University of Rochester Medical Center Strong Memorial — Rochester, New York
• SUNY Upstate Medical University — Syracuse, New York
• University of North Carolina at Chapel Hill — Chapel Hill, North Carolina

💰 Cost, Insurance & Patient Rights

• 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
• Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
• Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

More studies in Pregnancy Related

• Building TrUst and UNiting Teams Through DouLa partnErship - BUNDLE — Milwaukee, Wisconsin
• Trial of Community-based Patient Navigation — Atlanta, Georgia
• Study to Compare Maternal, Fetal, and Infant Outcomes of Women With Mild to Moderate Atopic Dermatitis Exposed to Ruxolitinib Cream During Pregnancy With an Unexposed Control Population — Morrisville, North Carolina
• Impact of Lactation Antenatal Teaching by Clinicians and Healthcare Providers — Loma Linda, California
• PRospective Evaluation of Peripartum Anticoagulation ManaGement for ThrOmboembolism — Durham, North Carolina
• Natural Versus Programmed Frozen Embryo Transfer (NatPro) — San Francisco, California

Explore by condition: All Pregnancy Related clinical trials

💡 How to Participate

1. Check the checklist above to see if you may qualify.
2. Review the official NIH record below to find the coordinating site.
3. Ask about the visit schedule, what is covered at no cost, and any travel support.
4. Confirm with your own doctor before making a decision.