ID
16573
Descripción
Study Sponsor: Astellas Study Title Tolerability of QUTENZA™ When Applied After Pre-treatment With Lidocaine or Tramadol in Subjects With Peripheral Neuropathic Pain - A Randomized, Multi-center, Assessor-blinded Study Medicine or Vaccine (generic name) capsaicin Sponsor Identification Number QTZ-EC-0002 Trial Registry Identification Number(#'s) NCT01416116 EudraCT Number: 2010-023258-34 Medical Condition Neuropathic pain Phase Phase 4 http://clinicaltrials.gov/show/NCT01416116 Treatment: Randomization Vital Signs: 75 mins prior to patch application Vital Signs: 15 mins prior to patch application Post patch application and post patch removal
Link
http://clinicaltrials.gov/show/NCT01416116
Palabras clave
Versiones (2)
- 24/7/16 24/7/16 -
- 11/8/16 11/8/16 -
Subido en
24 de julio de 2016
DOI
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Licencia
Creative Commons BY-NC 3.0
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Treatment Visit 2 Tolerability of QUTENZA™ When Applied After Pre-treatment With Lidocaine or Tramadol in Subjects With Peripheral Neuropathic Pain - A Randomized, Multi-center, Assessor-blinded Study NCT01416116
Treatment Visit 2 Tolerability of QUTENZA™ When Applied After Pre-treatment With Lidocaine or Tramadol in Subjects With Peripheral Neuropathic Pain - A Randomized, Multi-center, Assessor-blinded Study NCT01416116
Descripción
Vital Signs: 75 mins prior to patch application
Descripción
Assessment Date
Tipo de datos
date
Alias
- UMLS CUI [1]
- C2985720
Descripción
Scheduled Time
Tipo de datos
time
Alias
- UMLS CUI [1]
- C0086960
Descripción
Assessment Time
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C0040223
Descripción
Position
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0733755
Descripción
For any AE, please provide details on the 'Adverse Event' form.
Tipo de datos
text
Unidades de medida
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Descripción
Diastolic Blood Pressure
Tipo de datos
text
Unidades de medida
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Descripción
Record any clinically significant abnormal findings/conditions identified during the exam on the Current Medical and Surgical History and/or Adverse Event form.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0232117
Descripción
Vital Signs: 15 mins prior to patch application
Descripción
Assessment Date
Tipo de datos
date
Alias
- UMLS CUI [1]
- C2985720
Descripción
Scheduled Time
Tipo de datos
time
Alias
- UMLS CUI [1]
- C0086960
Descripción
Assessment Time
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C0040223
Descripción
Position
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0733755
Descripción
For any AE, please provide details on the 'Adverse Event' form.
Tipo de datos
text
Unidades de medida
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Descripción
Diastolic Blood Pressure
Tipo de datos
text
Unidades de medida
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Descripción
Record any clinically significant abnormal findings/conditions identified during the exam on the Current Medical and Surgical History and/or Adverse Event form.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0232117
Descripción
Vital Signs: Post patch application and post patch rGeemnoevraatl
Descripción
Assessment Date
Tipo de datos
date
Alias
- UMLS CUI [1]
- C2985720
Descripción
Scheduled Time
Tipo de datos
time
Alias
- UMLS CUI [1]
- C0086960
Descripción
Assessment Time
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C0040223
Descripción
Position
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0733755
Descripción
For any AE, please provide details on the 'Adverse Event' form.
Tipo de datos
text
Unidades de medida
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Descripción
Diastolic Blood Pressure
Tipo de datos
text
Unidades de medida
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Descripción
Record any clinically significant abnormal findings/conditions identified during the exam on the Current Medical and Surgical History and/or Adverse Event form.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0232117
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Treatment Visit 2 Tolerability of QUTENZA™ When Applied After Pre-treatment With Lidocaine or Tramadol in Subjects With Peripheral Neuropathic Pain - A Randomized, Multi-center, Assessor-blinded Study NCT01416116
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