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PubPharm (44)
1
Vil iltbehandling til en iltmætning på 88-92% sammenlignet med iltbehandling til en iltmætning på >94% reducere dødeligheden for patienter med kronisk obstruktiv lungesygdom med akut forværring? - et randomiseret klinisk forsøg : Will titrated oxygen flow to a peripheral oxygen saturation of 88-92% compared with oxygen flow to a saturation >94% reduce mortality in Chronic Obstructive Pulmonary Disease patients with acute exacerbation? – a randomized clinical trial
enthalten in:
WHO International Clinical Trials Registry Platform
| 2023
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2
Vil iltbehandling til en iltmætning på 88-92% sammenlignet med iltbehandling til en iltmætning på >94% reducere dødeligheden for patienter med kronisk obstruktiv lungesygdom med akut forværring? - et randomiseret klinisk forsøg : Will titrated oxygen flow to a peripheral oxygen saturation of 88-92% compared with oxygen flow to a saturation >94% reduce mortality in Chronic Obstructive Pulmonary Disease patients with acute exacerbation? – a randomized clinical trial
enthalten in:
WHO International Clinical Trials Registry Platform
| 2023
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3
En åben fase II undersøgelse af sikkerhed, tolerabilitet, højeste tolerable dosis og anti-tumor effekt af SCO-101 i kombination med FOLFIRI som en sikker og effektiv behandling af patienter med udbredt kolorektalkræft, der har udviklet behandlingsresistens overfor behandling med FOLFIRI : An?open-label phase II prospective clinical trial to?investigate safety, tolerability, maximum tolerated dose and anti-tumor?effect for SCO-101 in combination with?FOLFIRI?as?a safe and efficient treatment modality?in metastatic or advanced colorectal cancer (mCRC) patients with acquired?FOLFIRI?resistant cancer disease.
enthalten in:
WHO International Clinical Trials Registry Platform
| 2022
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4
En åben fase II undersøgelse af sikkerhed, tolerabilitet, højeste tolerable dosis og anti-tumor effekt af SCO-101 i kombination med FOLFIRI som en sikker og effektiv behandling af patienter med udbredt kolorektalkræft, der har udviklet behandlingsresistens overfor behandling med FOLFIRI : An?open-label phase II prospective clinical trial to?investigate safety, tolerability, maximum tolerated dose and anti-tumor?effect for SCO-101 in combination with?FOLFIRI?as?a safe and efficient treatment modality?in metastatic or advanced colorectal cancer (mCRC) patients with acquired?FOLFIRI?resistant cancer disease.
enthalten in:
WHO International Clinical Trials Registry Platform
| 2022
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5
Heparin dose (300 IU/kg vs. 600 IU/kg) in coroanry artery bypass grafting : Heparin dose (300 IU/kg vs. 600 IU/kg) in coroanry artery bypass grafting
enthalten in:
WHO International Clinical Trials Registry Platform
| 2019
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6
Heparin dose (300 IU/kg vs. 600 IU/kg) in coroanry artery bypass grafting : Heparin dose (300 IU/kg vs. 600 IU/kg) in coroanry artery bypass grafting
enthalten in:
WHO International Clinical Trials Registry Platform
| 2019
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7
IFM 2017-03 : A Phase 3 Study Comparing Lenalidomide and Daratumumab Subcutaneous Injection (R-Dara SC) vs Lenalidomide and Dexamethasone (Rd) in Frail Subjects with Previously Untreated Multiple Myeloma who are Ineligible for High Dose Therapy
enthalten in:
WHO International Clinical Trials Registry Platform
| 2019
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8
IFM 2017-03 : A Phase 3 Study Comparing Lenalidomide and Daratumumab Subcutaneous Injection (R-Dara SC) vs Lenalidomide and Dexamethasone (Rd) in Frail Subjects with Previously Untreated Multiple Myeloma who are Ineligible for High Dose Therapy
enthalten in:
WHO International Clinical Trials Registry Platform
| 2019
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9
uPAR PET/CT og FDG PET/CT til præoperativ stadieinddeling af patienter med nydiagnosticeret Gynækologisk Kræft : Phase II trial: uPAR PET/CT and FDG PET/CT for preoperative staging of gynecological cancers
enthalten in:
WHO International Clinical Trials Registry Platform
| 2018
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10
uPAR PET/CT og FDG PET/CT til præoperativ stadieinddeling af patienter med nydiagnosticeret Gynækologisk Kræft : Phase II trial: uPAR PET/CT and FDG PET/CT for preoperative staging of gynecological cancers
enthalten in:
WHO International Clinical Trials Registry Platform
| 2018
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Study Type: Interventional
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