CompletedNot applicableNCT03948958
PREMO Study: to Investigate Port REMoval Outcomes
Studying Cystic fibrosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Universitaire Ziekenhuizen KU Leuven
- Principal Investigator
- Marguerite Stas, MD, PhDUniversitaire Ziekenhuizen KU Leuven
- Intervention
- Evaluation of the catheter function(other)
- Enrollment
- 100 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2019 – 2022
Study locations (1)
- University Hospitals Leuven, Leuven, Belgium
Collaborators
B. Braun Medical SA
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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