ID
16867
Description
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 Visit Form 2/5: 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
Keywords
Versions (2)
- 7/24/16 7/24/16 -
- 8/11/16 8/11/16 -
Uploaded on
August 11, 2016
DOI
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License
Creative Commons BY 4.0
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Treatment Visit Form 2/5 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 Form 2/5 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
Description
Vital Signs: 75 mins prior to patch application
Description
Assessment Date
Data type
date
Alias
- UMLS CUI [1]
- C2985720
Description
Scheduled Time
Data type
time
Alias
- UMLS CUI [1]
- C0086960
Description
Assessment Time
Data type
time
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C0040223
Description
Position
Data type
integer
Alias
- UMLS CUI [1]
- C0733755
Description
For any AE, please provide details on the 'Adverse Event' form.
Data type
text
Measurement units
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Description
Diastolic Blood Pressure
Data type
text
Measurement units
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Description
Record any clinically significant abnormal findings/conditions identified during the exam on the Current Medical and Surgical History and/or Adverse Event form.
Data type
integer
Alias
- UMLS CUI [1]
- C0232117
Description
Vital Signs: 15 mins prior to patch application
Description
Assessment Date
Data type
date
Alias
- UMLS CUI [1]
- C2985720
Description
Scheduled Time
Data type
time
Alias
- UMLS CUI [1]
- C0086960
Description
Assessment Time
Data type
time
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C0040223
Description
Position
Data type
integer
Alias
- UMLS CUI [1]
- C0733755
Description
For any AE, please provide details on the 'Adverse Event' form.
Data type
text
Measurement units
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Description
Diastolic Blood Pressure
Data type
text
Measurement units
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Description
Record any clinically significant abnormal findings/conditions identified during the exam on the Current Medical and Surgical History and/or Adverse Event form.
Data type
integer
Alias
- UMLS CUI [1]
- C0232117
Description
Vital Signs: Post patch application and post patch rGeemnoevraatl
Description
Assessment Date
Data type
date
Alias
- UMLS CUI [1]
- C2985720
Description
Scheduled Time
Data type
time
Alias
- UMLS CUI [1]
- C0086960
Description
Assessment Time
Data type
time
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C0040223
Description
Position
Data type
integer
Alias
- UMLS CUI [1]
- C0733755
Description
For any AE, please provide details on the 'Adverse Event' form.
Data type
text
Measurement units
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Description
Diastolic Blood Pressure
Data type
text
Measurement units
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Description
Record any clinically significant abnormal findings/conditions identified during the exam on the Current Medical and Surgical History and/or Adverse Event form.
Data type
integer
Alias
- UMLS CUI [1]
- C0232117
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Treatment Visit Form 2/5 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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