ID
29900
Descrizione
Study ID: 102123 Clinical Study ID: FFR102123 Study Title: A randomised double-blind placebo controlled parallel group multicentre long term study to evaluate the safety of once-daily, intranasal administration of GW685698X aqueous nasal spray 100mcg* for 52 weeks in adult and adolescent subjects with perennial allergic rhinitis. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone furoate Trade Name: FLUTIDE, Allermist, Veramyst, FLUNASE, FLIXOTAIDE, FLUTAIDE, FLIXOVATE, Avamys; Veramyst, Avamys, Allermist Study Indication: Rhinitis, Allergic, Perennial This ODM-file contains Concomitant Medications.
Keywords
versioni (1)
- 26/04/18 26/04/18 - Sarah Riepenhausen
Titolare del copyright
GlaxoSmithKline
Caricato su
26 aprile 2018
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY-NC 3.0
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Safety of once-daily administration of Fluticasone nasal spray in adults and adolescents with perennial allergic rhinitis GSK 102123
Concomitant Medications
- StudyEvent: ODM
Descrizione
Non-Rhinitis Concomitant Medications
Alias
- UMLS CUI-1
- C2347852
- UMLS CUI-2
- C0205394
Descrizione
If Yes, record each medication in the following items of this itemgroup, use Trade Names where possible.
Tipo di dati
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0205394
Descrizione
Trade names are preferred
Tipo di dati
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2360065
Descrizione
Unit Dose
Tipo di dati
float
Alias
- UMLS CUI [1]
- C2826767
Descrizione
The following list of abbreviations are examples which can be used to aid the completion of this item. This is not an all inclusive list and is for guidance only, other abbreviations not listed may be used if necessary. ACTU = Actuation AMP = Amoule APP = Application BOT = Bottle CC = Cubic centimeter CAP = Capsule G = Gram GTT = Drops IU = International Units L = Litre L/MIN = Litres per minute LOZ = Lozenge MCG = Microgram MCG/KG/MIN = Microgram per kilogram per minute MCL = Microlitre MMOL = Millimole NEB = Nebule PUFF = Puff SPR = Spray TAB = Tablet TBLSP = Tablespoon TSP = Teaspoon % = Percent UNK = Unkown
Tipo di dati
text
Alias
- UMLS CUI [1]
- C2826646
Descrizione
The following list of abbreviations are examples which can be used to aid the completion of this item. The list is not all inclusive and is for guidance only, other abbreviations not listed may be used if necessary. OD/QD = 1 X daily BID = 2 X daily TID = 3 X daily QID = 4 X daily CONT = Continuous CUM = Cumulative dose D = Daily INT = Intermittent NA = Not available NOCT = At night OTH = Other PRN = As required QH = Every hour (quaque hora) QOD = Every other day QN = Every night (quaque nocte) SD = Single dose STAT = Immediately TAP = Taper UNK = Unknown
Tipo di dati
text
Alias
- UMLS CUI [1]
- C2826654
Descrizione
The following list of abbreviations are examples which can be used to aid the completion of this item. It is not all inclusive and is for guidance only, other abbreviations not listed may be used if necessary. IM = Intramuscular IH = Inhalation IN = Intranasal INJ = Injection IV = Intravenous NS = Nasal OTH = Other PO = Oral PR = Rectal SC = Subcutaneous TP = Topical UNK = Unknown
Tipo di dati
text
Alias
- UMLS CUI [1]
- C2826730
Descrizione
Ensure that the ’Reason for Medication’ is recorded on one of the following pages using the same terms: Current Medical Conditions (Medical and Allergy History), Non-Serious Adverse Events or Serious Adverse Events Form.
Tipo di dati
text
Alias
- UMLS CUI [1]
- C2826696
Descrizione
Check that either medication start date is completed or ’Taken Prior to Study?’ is ’Yes’. It is acceptable for start date to be missing if ’Taken Prior to Study?’ is ’Yes’. It is acceptable if ’Taken Prior to Study?’ is ’Yes’ and a start date is present, as long as the start date is prior to the date of the subject’s initial visit.
Tipo di dati
date
Alias
- UMLS CUI [1]
- C2826734
Descrizione
Check that either medication start date is completed or ’Taken Prior to Study?’ is ’Yes’. It is acceptable for start date to be missing if ’Taken Prior to Study?’ is ’Yes’. It is acceptable if ’Taken Prior to Study?’ is ’Yes’ and a start date is present, as long as the start date is prior to the date of the subject’s initial visit.
Tipo di dati
text
Alias
- UMLS CUI [1]
- C2826667
Descrizione
Check that either medication stop date is completed or ’Ongoing Medication?’ is ’Yes’. It is acceptable for stop date to be missing if ’Ongoing Medication?’ is ’Yes’.
Tipo di dati
date
Alias
- UMLS CUI [1]
- C2826744
Descrizione
Check that either medication stop date is completed or ’Ongoing Medication?’ is ’Yes’. It is acceptable for stop date to be missing if ’Ongoing Medication?’ is ’Yes’.
Tipo di dati
text
Alias
- UMLS CUI [1]
- C2826666
Similar models
Concomitant Medications
- StudyEvent: ODM
C0035455 (UMLS CUI-2)
C0035455 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])
C2607914 (UMLS CUI [1,3])
C2607914 (UMLS CUI [1,2])
C2607914 (UMLS CUI [1,2])
C2607914 (UMLS CUI [1,2])
C2607914 (UMLS CUI [1,2])
C2607914 (UMLS CUI [1,2])
C2607914 (UMLS CUI [1,2])
C2607914 (UMLS CUI [1,2])
C0205394 (UMLS CUI-2)
C0205394 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,2])