Use of Portable Technology in Patient Education of Shave/Punch Biopsies
NCT ID: NCT01110148
Last Updated: 2010-04-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
84 participants
INTERVENTIONAL
2009-07-31
2010-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Correlation of Dermatologist Made Biopsy Decision With AI Assisted Total Body Photography Detection of Outlier Lesions
NCT05940090
The INFORM Study: Rotational Fractional Resection for Submental Contouring
NCT03853980
Evaluation of Safety, PK, and Preliminary Effects on Scar Formation of Multiple Intradermal Administrations of RXI-109
NCT01780077
Evaluation of Age-Related Skin Changes
NCT03842566
Harmonics-based in Vivo Optical Virtual Biopsy
NCT01980264
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Video-based informed consent
patients receiving informed consent through video format
video-based informed consent for skin biopsies
video-based informed consent for punch and shave biopsies
traditional informed consent
patients receiving traditional informed consent from the physicians.
traditional informed consent
traditional informed consent (standard of care) from physicians for shave and punch biopsies
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
video-based informed consent for skin biopsies
video-based informed consent for punch and shave biopsies
traditional informed consent
traditional informed consent (standard of care) from physicians for shave and punch biopsies
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Receiving shave or punch biopsy
Exclusion Criteria
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of California, Davis
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
University of California, Davis
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
April W Armstrong, M.D.
Role: PRINCIPAL_INVESTIGATOR
UC Davis Health System
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University of California Davis Medical Center
Sacramento, California, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
200917169-1
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.