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journalStr:"WHO International Clinical Trials Registry Platform"
topic_facet:"Phase: Phase 4"
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PubPharm (618)
1
The Soft Tissue Injection of Corticosteroid and Local Anaesthetic Study : The Soft Tissue Injection of Corticosteroid And Local anaesthetic Study - A Single site, non-inferiority randomised control trial evaluating pain after soft tissue corticosteroid injections with and without local anaesthetic - The SToICAL Study
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| 2023
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2
The Soft Tissue Injection of Corticosteroid and Local Anaesthetic Study : The Soft Tissue Injection of Corticosteroid And Local anaesthetic Study - A Single site, non-inferiority randomised control trial evaluating pain after soft tissue corticosteroid injections with and without local anaesthetic - The SToICAL Study
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3
Randomized head-to-head trial of proton pump inhibitor (PPI) vs topical corticosteroids (TCs) post food bolus impaction and/or for untreated patients with Eosinophilic esophagitis (EoE). : Randomized head-to-head trial of proton pump inhibitor (PPI) vs topical corticosteroids (TCs) post food bolus impaction and/or for untreated patients with Eosinophilic esophagitis (EoE).
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4
Randomized head-to-head trial of proton pump inhibitor (PPI) vs topical corticosteroids (TCs) post food bolus impaction and/or for untreated patients with Eosinophilic esophagitis (EoE). : Randomized head-to-head trial of proton pump inhibitor (PPI) vs topical corticosteroids (TCs) post food bolus impaction and/or for untreated patients with Eosinophilic esophagitis (EoE).
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5
CORTICOSTEROID RANDOMISATION AFTER SIGNIFICANT HEAD INJURY : CORTICOSTEROID RANDOMISATION AFTER SIGNIFICANT HEAD INJURY
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6
A 26-WEEK, RANDOMIZED, DOUBLE-BLIND, PARALLEL-GROUP, ACTIVE CONTROLLED, MULTICENTER, MULTINATIONAL SAFETY STUDY EVALUATING THE RISK OF SERIOUS ASTHMA-RELATED EVENTS DURING TREATMENT WITH SYMBICORT® , A FIXED COMBINATION OF INHALED CORTICOSTEROID (ICS) (BUDESONIDE) AND A LONG ACTING ß2 - AGONIST (LABA)(FORMOTEROL) AS COMPARED TO TREATMENT WITH ICS (BUDESONIDE) ALONE IN ADULT AND ADOLESCENT (≥12 YEARS OF AGE) PATIENTS WITH ASTHMA. : A 26-WEEK, RANDOMIZED, DOUBLE-BLIND, PARALLEL-GROUP, ACTIVE CONTROLLED, MULTICENTER, MULTINATIONAL SAFETY STUDY EVALUATING THE RISK OF SERIOUS ASTHMA-RELATED EVENTS DURING TREATMENT WITH SYMBICORT® , A FIXED COMBINATION OF INHALED CORTICOSTEROID (ICS) (BUDESONIDE) AND A LONG ACTING ß2 - AGONIST (LABA)(FORMOTEROL) AS COMPARED TO TREATMENT WITH ICS (BUDESONIDE) ALONE IN ADULT AND ADOLESCENT (≥ 12 YEARS OF AGE) PATIENTS WITH ASTHMA.
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7
MULTIPLE COURSES OF ANTENATAL CORTICOSTEROIDS FOR PRETERM BIRTH STUDY (MACS) : MULTIPLE COURSES OF ANTENATAL CORTICOSTEROIDS FOR PRETERM BIRTH STUDY (MACS)
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8
A 52-WEEK, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFECT OF ROFLUMILAST 500 μg ON EXACERBATION RATE IN SUBJECTS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD) TREATED WITH A FIXED-DOSE COMBINATION OF LONG-ACTING BETA AGONIST AND INHALED CORTICOSTEROID (LABA/ICS) : A 52-WEEK, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFECT OF ROFLUMILAST 500 μg ON EXACERBATION RATE IN SUBJECTS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD) TREATED WITH A FIXED-DOSE COMBINATION OF LONG-ACTING BETA AGONIST AND INHALED CORTICOSTEROID (LABA/ICS)
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9
CORTICOSTEROID RANDOMISATION AFTER SIGNIFICANT HEAD INJURY : CORTICOSTEROID RANDOMISATION AFTER SIGNIFICANT HEAD INJURY
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10
A 26-WEEK, RANDOMIZED, DOUBLE-BLIND, PARALLEL-GROUP, ACTIVE CONTROLLED, MULTICENTER, MULTINATIONAL SAFETY STUDY EVALUATING THE RISK OF SERIOUS ASTHMA-RELATED EVENTS DURING TREATMENT WITH SYMBICORT® , A FIXED COMBINATION OF INHALED CORTICOSTEROID (ICS) (BUDESONIDE) AND A LONG ACTING ß2 - AGONIST (LABA)(FORMOTEROL) AS COMPARED TO TREATMENT WITH ICS (BUDESONIDE) ALONE IN ADULT AND ADOLESCENT (≥12 YEARS OF AGE) PATIENTS WITH ASTHMA. : A 26-WEEK, RANDOMIZED, DOUBLE-BLIND, PARALLEL-GROUP, ACTIVE CONTROLLED, MULTICENTER, MULTINATIONAL SAFETY STUDY EVALUATING THE RISK OF SERIOUS ASTHMA-RELATED EVENTS DURING TREATMENT WITH SYMBICORT® , A FIXED COMBINATION OF INHALED CORTICOSTEROID (ICS) (BUDESONIDE) AND A LONG ACTING ß2 - AGONIST (LABA)(FORMOTEROL) AS COMPARED TO TREATMENT WITH ICS (BUDESONIDE) ALONE IN ADULT AND ADOLESCENT (≥ 12 YEARS OF AGE) PATIENTS WITH ASTHMA.
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Zeitschrift: WHO International Clinical Trials Registry Platform
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Thema: Phase: Phase 4
Medienart
618
Aufsätze
618
E-Artikel
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WHO International Clinical Trials Registry Plat...
Thema
618
610
Phase: Phase 4
606
Study Type: Interventional
238
Recruitment Status: Not yet recruiting
140
Recruitment Status: Completed
116
Recruitment Status: Authorised-recruitment may ...
84
Recruitment Status: Recruiting
22
Medical Condition: ASTHMA UNCONTROLLED ON MEDIU...
12
Medical Condition: Asthma; Asthma;Respiratory -...
12
Medical Condition: Health Condition 1: O- Medic...
12
Study Type: Observational
8
Medical Condition: Asthma
8
Medical Condition: Prophylaxis of rejection in ...
8
Recruitment Status: Closed to Recruitment of Pa...
8
Recruitment Status: Complete: follow-up complete
6
Medical Condition: ;Diseases of the musculo-ske...
6
Medical Condition: Anaesthesia;Anaesthesia
6
Medical Condition: Health Condition 1: K011- Im...
4
Medical Condition: ;Neoplasms
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Medical Condition: ;Not Applicable
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166
2010-2019
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