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Cystic Fibrosis Latest Advances
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Last Updated: 02/19/2023
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Found 240 publications
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Interventions for the eradication of meticillin-resistant Staphylococcus aureus (MRSA) in people with cystic fibrosis.
Condition:
Meticillin-Resistant Staphylococcus Aureus (MRSA) in Patients with Cystic Fibrosis
Journal:
The Cochrane database of systematic reviews
Treatment Used:
Antimicrobials
Number of Patients:
0
Published:
December 13, 2022
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Effects of long-term tobramycin inhalation solution (TIS) once daily on exacerbation rate in patients with non-cystic fibrosis bronchiectasis.
Condition:
Bronchiectasis
Journal:
Respiratory research
Treatment Used:
Tobramycin Inhalation Solution (TIS)
Number of Patients:
58
Published:
December 03, 2022
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Inhaled anti-pseudomonal antibiotics for long-term therapy in cystic fibrosis.
Condition:
Cystic Fibrosis
Journal:
The Cochrane database of systematic reviews
Treatment Used:
Inhaled Anti-Pseudomonal Antibiotics
Number of Patients:
3042
Published:
November 14, 2022
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Antifungal therapies for allergic bronchopulmonary aspergillosis in people with cystic fibrosis.
Condition:
Allergic Bronchopulmonary Aspergillosis (ABPA) in Patients with Cystic Fibrosis
Journal:
The Cochrane database of systematic reviews
Treatment Used:
Antifungal Therapies
Number of Patients:
0
Published:
September 02, 2022
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Effectiveness of nebulized hypertonic saline in patients with bronchial hypersecretion.
Condition:
Bronchial Hypersecretion
Journal:
Medicina clinica
Treatment Used:
Nebulized Hypertonic Saline (HS)
Number of Patients:
101
Published:
August 05, 2022
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Biologic drugs in treating allergic bronchopulmonary aspergillosis in patients with cystic fibrosis: a systematic review.
Condition:
Allergic Bronchopulmonary Aspergillosis (ABPA) in Patients with Cystic Fibrosis (CF)
Journal:
European respiratory review : an official journal of the European Respiratory Society
Treatment Used:
Biologics
Number of Patients:
0
Published:
July 27, 2022
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Efficacy and Safety of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 Through 11 Years of Age with Cystic Fibrosis Heterozygous for F508del and a Minimal Function Mutation: A Phase 3b, Randomized, Placebo-controlled Study.
Condition:
Young Children with Cystic Fibrosis
Journal:
American journal of respiratory and critical care medicine
Treatment Used:
Elexacaftor/Tezacaftor/Ivacaftor
Number of Patients:
121
Published:
July 11, 2022
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A Phase 3, Open-Label Study of Lumacaftor/Ivacaftor in Children 1 to Less Than 2 Years of Age with Cystic Fibrosis Homozygous for F508del-CFTR.
Condition:
Children 1 to Less Than 2 Years of Age with Cystic Fibrosis (CF)
Journal:
American journal of respiratory and critical care medicine
Treatment Used:
Lumacaftor/Ivacaftor
Number of Patients:
44
Published:
June 30, 2022
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The effect of azithromycin on structural lung disease in infants with cystic fibrosis (COMBAT CF): a phase 3, randomised, double-blind, placebo-controlled clinical trial.
Condition:
Structural Lung Disease in Infants with Cystic Fibrosis (CF)
Journal:
The Lancet. Respiratory medicine
Treatment Used:
Azithromycin
Number of Patients:
281
Published:
June 06, 2022
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Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on Lung Clearance Index and Magnetic Resonance Imaging in Patients with Cystic Fibrosis and One or Two F508del Alleles.
Condition:
Cystic Fibrosis (CF)
Journal:
American journal of respiratory and critical care medicine
Treatment Used:
Elexacaftor/Tezacaftor/Ivacaftor Therapy
Number of Patients:
91
Published:
May 10, 2022
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Translated article Aquagenic Keratoderma: Treatment Update.
Condition:
Aquagenic Keratoderma
Journal:
Actas dermo-sifiliograficas
Treatment Used:
Multiple Treatments
Published:
May 08, 2022
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Results of Lung Transplantations Among Cystic Fibrosis Patients: A Single-Center Study.
Condition:
Cystic Fibrosis (CF)
Journal:
Transplantation proceedings
Treatment Used:
Lung Transplantation
Number of Patients:
56
Published:
May 02, 2022
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Showing 1-12 of 240
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Last Updated: 02/19/2023