ID
16871
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 End of Study Form 1/: Vital Signs Identification of Painful Area: Change NPRS 'average pain' score NPRS 'pain now' score Adverse Event 1 Concomitant Medication 1 Any Non-medication Therapy
Lien
http://clinicaltrials.gov/show/NCT01416116
Mots-clés
Versions (1)
- 11/08/2016 11/08/2016 -
Téléchargé le
11 août 2016
DOI
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Licence
Creative Commons BY 4.0
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End of Study Form 1/ 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
End of Study Form 1/ 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
Identification of Painful Area: Change
Description
NPRS 'average pain' score
Description
Date of Assessment
Type de données
date
Alias
- UMLS CUI [1]
- C2985720
Description
NPRS 'average' pain score
Type de données
integer
Alias
- UMLS CUI [1]
- C0582148
Description
NPRS 'pain now' score: Post patch application and post patch removal
Description
Date of Assessment
Type de données
date
Alias
- UMLS CUI [1]
- C2985720
Description
NPRS 'pain now' score
Type de données
integer
Alias
- UMLS CUI [1]
- C0582148
Description
Tolerability score: Post patch removal
Description
Date of Assessment
Type de données
date
Alias
- UMLS CUI [1]
- C2985720
Description
120 mins post patch removal
Type de données
integer
Alias
- UMLS CUI [1]
- C3274448
Description
Additional Information
Description
If 'Yes', please provide details on 'Adverse Event' form.
Type de données
integer
Alias
- UMLS CUI [1]
- C0877248
Description
Concomitant medication
Type de données
integer
Alias
- UMLS CUI [1]
- C2347852
Description
If 'Yes', please provide details on 'Non-medication Therapy' form.
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C1518422
Similar models
End of Study Form 1/ 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
C0392747 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
C1518422 (UMLS CUI [1,3])