ID
4905
Beschrijving
ODM derived from http://clinicaltrials.gov/show/NCT00332709
Link
http://clinicaltrials.gov/show/NCT00332709
Trefwoorden
Versies (4)
- 11-12-13 11-12-13 - Martin Dugas
- 14-04-14 14-04-14 - Julian Varghese
- 02-09-21 02-09-21 -
- 20-09-21 20-09-21 -
Geüploaded op
14 april 2014
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
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Eligibility NCT00332709 Osteoporosis. Postmenopausal
Eligibility
- StudyEvent: Eligibility
Beschrijving
Ausschlusskriterien
Alias
- UMLS CUI 2011AA
- CL425201
Beschrijving
Estrogen- and progesterone-receptor status negative or unknown
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C1516974
- UMLS CUI 2011AA
- CL415098
- UMLS CUI 2011AA
- C0279758
- UMLS CUI 2011AA
- C1514471
- UMLS CUI 2011AA
- CL415098
- UMLS CUI 2011AA
- C0279768
Beschrijving
Completion of adjuvant tamoxifen therapy more than 6 months prior to study start
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0580352
- SNOMED CT 2011_0131
- 182992009
- UMLS CUI 2011AA
- C1522673
- UMLS CUI 2011AA
- C0039286
- SNOMED CT 2011_0131
- 373345002
- LOINC Version 232
- MTHU003102
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C2348558
Beschrijving
Inflammatory breast cancer
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0278601
- SNOMED CT 2011_0131
- 254840009
- MedDRA 14.1
- 10021980
Beschrijving
Current/active dental problems including infection of the teeth or jawbone, dental or fixture trauma, or a current or prior diagnosis of osteonecrosis of the jaw, of exposed bone in the mouth, or of slow healing after dental procedures
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0521116
- SNOMED CT 2011_0131
- 15240007
- UMLS CUI 2011AA
- C0205177
- SNOMED CT 2011_0131
- 55561003
- UMLS CUI 2011AA
- C1704330
- SNOMED CT 2011_0131
- 105995000
- MedDRA 14.1
- 10012322
- ICD-10-CM Version 2010
- K08.9
- ICD-9-CM Version 2011
- 525.9
- UMLS CUI 2011AA
- CL425202
- UMLS CUI 2011AA
- C0877046
- SNOMED CT 2011_0131
- 427898007
- MedDRA 14.1
- 10048762
- CTCAE 1105E
- E11594
- UMLS CUI 2011AA
- C1400570
- UMLS CUI 2011AA
- C1301685
- SNOMED CT 2011_0131
- 397869004
- UMLS CUI 2011AA
- C2363483
- UMLS CUI 2011AA
- C0175677
- SNOMED CT 2011_0131
- 417746004
- MedDRA 14.1
- 10022116
- ICD-10-CM Version 2010
- T14.9
- UMLS CUI 2011AA
- C0521116
- SNOMED CT 2011_0131
- 15240007
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C0011900
- SNOMED CT 2011_0131
- 439401001
- LOINC Version 232
- MTHU008876
- UMLS CUI 2011AA
- C1401381
- MedDRA 14.1
- 10064658
- CTCAE 1105E
- E12502
- UMLS CUI 2011AA
- CL428750
- MedDRA 14.1
- 10071014
- UMLS CUI 2011AA
- C0439834
- SNOMED CT 2011_0131
- 255361000
- UMLS CUI 2011AA
- C2004454
- UMLS CUI 2011AA
- C0231290
- SNOMED CT 2011_0131
- 237679004, 255234002
- UMLS CUI 2011AA
- C0011331
- SNOMED CT 2011_0131
- 108306002
- MedDRA 14.1
- 10061813
- LOINC Version 232
- MTHU015835
Beschrijving
Recent (within 6 weeks) or planned dental or jaw surgery
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0332185
- SNOMED CT 2011_0131
- 6493001
- UMLS CUI 2011AA
- C1301732
- SNOMED CT 2011_0131
- 397943006
- UMLS CUI 2011AA
- C0204324
- SNOMED CT 2011_0131
- 81733005
- MedDRA 14.1
- 10061812
- UMLS CUI 2011AA
- C0524861
- MedDRA 14.1
- 10051059
Beschrijving
History of diseases with influence on bone metabolism such as Paget's disease and primary overactive parathyroid
Datatype
boolean
Alias
- UMLS CUI 2011AA
- CL421546
- SNOMED CT 2011_0131
- 392521001
- UMLS CUI 2011AA
- C0012634
- SNOMED CT 2011_0131
- 64572001
- UMLS CUI 2011AA
- C0814606
- UMLS CUI 2011AA
- C0596204
- UMLS CUI 2011AA
- C1368019
- UMLS CUI 2011AA
- CL414904
- UMLS CUI 2011AA
- C0443272
- SNOMED CT 2011_0131
- 263829006
- MedDRA 14.1
- 10033288
- UMLS CUI 2011AA
- C0030517
- SNOMED CT 2011_0131
- 73132005
- MedDRA 14.1
- 10033942
- ICD-10-CM Version 2010
- E21.5
- ICD-9-CM Version 2011
- 252.9
Beschrijving
Prior or concomitant therapies: chemotherapy within the last 12 months, intravenous or oral bisphosphonates, systemic corticosteroids, anabolic steroids or growth hormones, Tibolone, parathyroid hormone, systemic sodium fluoride or any drugs known to affect the skeleton (such as calcitonin, mithramycin, or gallium nitrate)
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- CL415222
- UMLS CUI 2011AA
- C0039798
- UMLS CUI 2011AA
- C0392920
- SNOMED CT 2011_0131
- 150415003
- UMLS CUI 2011AA
- C0348016
- SNOMED CT 2011_0131
- 255560000
- UMLS CUI 2011AA
- C1527415
- SNOMED CT 2011_0131
- 26643006
- HL7 V3 2006_05
- _OralRoute
- UMLS CUI 2011AA
- C0012544
- SNOMED CT 2011_0131
- 372907000
- UMLS CUI 2011AA
- C0205373
- SNOMED CT 2011_0131
- 31099001
- UMLS CUI 2011AA
- C0001617
- SNOMED CT 2011_0131
- 79440004
- UMLS CUI 2011AA
- C0002744
- SNOMED CT 2011_0131
- 111151007
- LOINC Version 232
- MTHU019429
- UMLS CUI 2011AA
- C1258800
- UMLS CUI 2011AA
- C0037663
- SNOMED CT 2011_0131
- 56234005
- LOINC Version 232
- MTHU002890
- UMLS CUI 2011AA
- C0076660
- SNOMED CT 2011_0131
- 395903002
- UMLS CUI 2011AA
- C0030520
- SNOMED CT 2011_0131
- 4076007
- LOINC Version 232
- MTHU005026
- UMLS CUI 2011AA
- C0205373
- SNOMED CT 2011_0131
- 31099001
- UMLS CUI 2011AA
- C0037508
- SNOMED CT 2011_0131
- 6910009
- UMLS CUI 2011AA
- C0013227
- UMLS CUI 2011AA
- C0205309
- SNOMED CT 2011_0131
- 36692007
- UMLS CUI 2011AA
- C0814606
- UMLS CUI 2011AA
- C1283922
- SNOMED CT 2011_0131
- 361378004
- UMLS CUI 2011AA
- C0006668
- SNOMED CT 2011_0131
- 63730009
- LOINC Version 232
- MTHU003443
- UMLS CUI 2011AA
- C0026234
- SNOMED CT 2011_0131
- 387101002
- UMLS CUI 2011AA
- C0061008
- SNOMED CT 2011_0131
- 109092007
Beschrijving
Patients with previous or concomitant cancers (not breast cancer) within the past 5 years EXCEPT adequately treated basal or squamous cell skin cancers or in situ cancer of the cervix. Patients with previous other cancer(s) must have been disease-free for at least 5 years.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0205156
- SNOMED CT 2011_0131
- 9130008
- UMLS CUI 2011AA
- CL415222
- UMLS CUI 2011AA
- C0006826
- SNOMED CT 2011_0131
- 363346000
- MedDRA 14.1
- 10028997
- LOINC Version 232
- MTHU010328
- ICD-10-CM Version 2010
- C00-C96
- UMLS CUI 2011AA
- C1518422
- UMLS CUI 2011AA
- C0678222
- SNOMED CT 2011_0131
- 254838004
- MedDRA 14.1
- 10006204
- UMLS CUI 2011AA
- C1554961
- HL7 V3 2006_05
- E
- UMLS CUI 2011AA
- C0205411
- SNOMED CT 2011_0131
- 88323005
- UMLS CUI 2011AA
- CL415147
- UMLS CUI 2011AA
- C0007117
- SNOMED CT 2011_0131
- 1338007
- MedDRA 14.1
- 10004146
- UMLS CUI 2011AA
- C0553723
- SNOMED CT 2011_0131
- 254651007
- MedDRA 14.1
- 10041834
- UMLS CUI 2011AA
- C0851140
- SNOMED CT 2011_0131
- 92564006
- MedDRA 14.1
- 10061809
- ICD-10-CM Version 2010
- D06.9
- ICD-9-CM Version 2011
- 233.1
- UMLS CUI 2011AA
- C0332288
- SNOMED CT 2011_0131
- 45169001
- UMLS CUI 2011AA
- C0012634
- SNOMED CT 2011_0131
- 64572001
Beschrijving
Patients currently receiving oral bisphosphonates must discontinue these at least 3 weeks prior to study start.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0521116
- SNOMED CT 2011_0131
- 15240007
- UMLS CUI 2011AA
- C1514756
- UMLS CUI 2011AA
- C1527415
- SNOMED CT 2011_0131
- 26643006
- HL7 V3 2006_05
- _OralRoute
- UMLS CUI 2011AA
- C0012544
- SNOMED CT 2011_0131
- 372907000
- UMLS CUI 2011AA
- C0457454
- SNOMED CT 2011_0131
- 278308006
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C2348558
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