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topic_facet:"Phase: Phase 3"
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PubPharm (12)
1
N/A - EXAFIP : N/A - EXAFIP
enthalten in:
WHO International Clinical Trials Registry Platform
| 2021
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2
N/A - EXAFIP : N/A - EXAFIP
enthalten in:
WHO International Clinical Trials Registry Platform
| 2021
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3
PRAVAPREV-01 : A Double blind randomized phase III study of pravastatin vs placebo as primary prevention of severe subcutaneous breast fibrosis in hyper-radiosensitive identified patients with breast cancer - PRAVAPREV-01
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WHO International Clinical Trials Registry Platform
| 2021
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4
PRAVAPREV-01 : A Double blind randomized phase III study of pravastatin vs placebo as primary prevention of severe subcutaneous breast fibrosis in hyper-radiosensitive identified patients with breast cancer - PRAVAPREV-01
enthalten in:
WHO International Clinical Trials Registry Platform
| 2021
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5
Hypertonic saline during hospitalisation in Cystic Fibrosis study : Phase 3, placebo-controlled, parallel-group, randomised trial of the effect of nebulised hypertonic saline on the length of stay of people hospitalised with acute exacerbations of Cystic Fibrosis lung disease.
enthalten in:
WHO International Clinical Trials Registry Platform
| 2020
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6
Hypertonic saline during hospitalisation in Cystic Fibrosis study : Phase 3, placebo-controlled, parallel-group, randomised trial of the effect of nebulised hypertonic saline on the length of stay of people hospitalised with acute exacerbations of Cystic Fibrosis lung disease.
enthalten in:
WHO International Clinical Trials Registry Platform
| 2020
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7
MRSA study. : Early eradication of S. Aureus (MRSA) in patients with cystic fibrosis: a randomized multicenter study.
enthalten in:
WHO International Clinical Trials Registry Platform
| 2018
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8
MRSA study. : Early eradication of S. Aureus (MRSA) in patients with cystic fibrosis: a randomized multicenter study.
enthalten in:
WHO International Clinical Trials Registry Platform
| 2018
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9
Tiotropium-bromide in cystic fibrosic : A randomised, double-blind, placebo-controlled parallel-group trial to confirm the efficacy after 12 weeks and the safety of tiotropium 5 µg administered once daily via the Respimat® device in patients with cystic fibrosis.
enthalten in:
WHO International Clinical Trials Registry Platform
| 2017
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10
Tiotropium-bromide in cystic fibrosic : A randomised, double-blind, placebo-controlled parallel-group trial to confirm the efficacy after 12 weeks and the safety of tiotropium 5 µg administered once daily via the Respimat® device in patients with cystic fibrosis.
enthalten in:
WHO International Clinical Trials Registry Platform
| 2017
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Thema: Phase: Phase 3
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WHO International Clinical Trials Registry Plat...
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Phase: Phase 3
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Study Type: Interventional
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Recruitment Status: Not yet recruiting
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Recruitment Status: Authorised-recruitment may ...
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Medical Condition: Cystic Fibrosis MedDRA versi...
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Medical Condition: Cystic fibrosis; Cystic fibr...
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Medical Condition: Idiopathic Pulmonary Fibrosi...
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Medical Condition: MedDRA version: 18.0Level: L...
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Medical Condition: Radio-induced fibrosis in br...
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Recruitment Status: Withdrawn
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2010-2019
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