PRURITCC: Itch and Pain Characteristics in Skin Carcinomas
Sponsor
University Hospital, Brest (Other)
Overall Status
Completed
CT.gov ID
NCT03290989
Collaborator
(none)
100
1
4
25.2
Study Details
Study Description
Brief Summary
The objective of this study is to have better knowledge about sensations of patients with skin carcinomas and to have data about characteristics of pain and pruritus . All patients presenting with a suspicions lesion for skin carcinomas will be included and will respond to a questionnaire. Demographics data, and histological data about skin carcinomas will be collected.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Study Design
Study Type:
Observational
Actual Enrollment
:
100 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Itch and Pain Characteristics in Skin Carcinomas
Actual Study Start Date
:
Apr 1, 2015
Actual Primary Completion Date
:
Apr 1, 2015
Actual Study Completion Date
:
Jul 31, 2015
Outcome Measures
Primary Outcome Measures
- Evaluate characteristics of pruritus in skin carcinomas [Day1 (when presenting at consultation with a skin lesion suspicious for carcinoma)]
Questions about characteristics
- Evaluate characteristics of pruritus in skin carcinomas [Day1 (when presenting at consultation with a skin lesion suspicious for carcinoma]
Numerical visual scale (EVA)
- Evaluate characteristics of pruritus in skin carcinomas [Day1 (when presenting at consultation with a skin lesion suspicious for carcinoma]
5D-itch scale
- Evaluate characteristics of pain in skin carcinomas [Day1 (when presenting at consultation with a skin lesion suspicious for carcinoma]
Numerical visual pain
- Evaluate characteristics of in skin carcinomas [Day1 (when presenting at consultation with a skin lesion suspicious for carcinoma]
score DN4
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
all patients with suspected skin carcinoma aged 18 years or more
Exclusion Criteria:
-
age under 18 years,
-
inability to complete the questionnaire because of cognitive impairment
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | CHRU de Brest | Brest | France | 29609 |
Sponsors and Collaborators
- University Hospital, Brest
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
University Hospital, Brest
ClinicalTrials.gov Identifier:
NCT03290989
Other Study ID Numbers:
- PRURITCC
First Posted:
Sep 25, 2017
Last Update Posted:
Sep 25, 2017
Last Verified:
Sep 1, 2017
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms: