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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01632644
Other study ID # STU66384
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 2012
Est. completion date May 2013

Study information

Verified date December 2021
Source Northwestern University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The primary objective of this study is to investigate the patient experience during skin biopsy.


Recruitment information / eligibility

Status Completed
Enrollment 59
Est. completion date May 2013
Est. primary completion date May 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age 18 and Over - The subjects are in good health. - The subjects have the willingness and the ability to understand and provide informed consent for the use of their tissue and communicate with the investigator. - Patients who have had one or multiple skin biopsies OR board-certified dermatologists. Exclusion Criteria: - Under 18 years of age. - Subjects who are unable to understand the protocol or give informed consent.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Survey/Interview
Each group will be surveyed and interviewed.

Locations

Country Name City State
United States Northwestern University Dermatology Chicago Illinois

Sponsors (1)

Lead Sponsor Collaborator
Northwestern University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Review of Physician and Patient Experience Subjects will answer a combination of:
Open-ended questions and
Questions asking for subject to rank possible responses
Last four weeks of study
Secondary Physician's Experience with Skin Biopsy Sites Physicians will answer a combination of:
Open-ended questions, and
Questions asking for subject to rank possible responses
First four weeks of study
Secondary Patient's Experience with Skin Biopsy Sites Patients will answer a combination of:
Open-ended questions and
Questions asking for subject to rank possible responses
First four weeks of study