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Last Updated: 02/19/2023

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Found 240 publications

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

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

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

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

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

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

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

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

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

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

Translated article Aquagenic Keratoderma: Treatment Update.

Condition: Aquagenic Keratoderma
Journal: Actas dermo-sifiliograficas
Treatment Used: Multiple Treatments
Published: May 08, 2022

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
Showing 1-12 of 240

Last Updated: 02/19/2023