ID
29900
Beschrijving
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.
Trefwoorden
Versies (1)
- 26-04-18 26-04-18 - Sarah Riepenhausen
Houder van rechten
GlaxoSmithKline
Geüploaded op
26 april 2018
DOI
Voor een aanvraag inloggen.
Licentie
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
Beschrijving
Non-Rhinitis Concomitant Medications
Alias
- UMLS CUI-1
- C2347852
- UMLS CUI-2
- C0205394
Beschrijving
If Yes, record each medication in the following items of this itemgroup, use Trade Names where possible.
Datatype
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0205394
Beschrijving
Trade names are preferred
Datatype
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2360065
Beschrijving
Unit Dose
Datatype
float
Alias
- UMLS CUI [1]
- C2826767
Beschrijving
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
Datatype
text
Alias
- UMLS CUI [1]
- C2826646
Beschrijving
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
Datatype
text
Alias
- UMLS CUI [1]
- C2826654
Beschrijving
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
Datatype
text
Alias
- UMLS CUI [1]
- C2826730
Beschrijving
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.
Datatype
text
Alias
- UMLS CUI [1]
- C2826696
Beschrijving
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.
Datatype
date
Alias
- UMLS CUI [1]
- C2826734
Beschrijving
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.
Datatype
text
Alias
- UMLS CUI [1]
- C2826667
Beschrijving
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’.
Datatype
date
Alias
- UMLS CUI [1]
- C2826744
Beschrijving
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’.
Datatype
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])