Investigating Clinical Trial Participation for Acne Patients
An Assessment of Clinical Trial Experiences of Patients With Acne
1 other identifier
observational
500
0 countries
N/A
Brief Summary
Participation in medical trials usually favors a particular demographic group. But there is limited research available to explain what trial attributes affect the completion of these specific demographic groups. This trial will scrutinize the experiences of patients diagnosed with acne as they take part in a separate medical intervention clinical trial. The focus will be on tracking the rates of completion and withdrawal among these individuals. It will also try to analyze data from the perspective of different demographic groups to check for recurring trends which might yield insights for the sake of future acne patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2024
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 10, 2023
CompletedFirst Posted
Study publicly available on registry
February 21, 2023
CompletedStudy Start
First participant enrolled
March 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2026
CompletedJune 5, 2023
June 1, 2023
1 year
February 10, 2023
June 2, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Number of acne patients who decide to join in a clinical study
3 months
Rate of patients who remain in an acne clinical study to completion
12 months
Eligibility Criteria
Acne patients who are actively participating in a clinical study, but have not yet completed enrollment and randomization.
You may qualify if:
- Patient has been diagnosed with acne
- Patient is able to read, understand and provide written Informed Consent
- Patient is a minimum of 18 years or older
You may not qualify if:
- Inability to perform regular electronic reporting
- Pregnant or lactating women
- Has significant intercurrent illness, psychiatric disposition or other factors that, in the opinion of the Investigator or Medical Monitor, precludes participation in the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (3)
Eichenfield DZ, Sprague J, Eichenfield LF. Management of Acne Vulgaris: A Review. JAMA. 2021 Nov 23;326(20):2055-2067. doi: 10.1001/jama.2021.17633.
PMID: 34812859BACKGROUNDWilliams HC, Dellavalle RP, Garner S. Acne vulgaris. Lancet. 2012 Jan 28;379(9813):361-72. doi: 10.1016/S0140-6736(11)60321-8. Epub 2011 Aug 29.
PMID: 21880356BACKGROUNDTitus S, Hodge J. Diagnosis and treatment of acne. Am Fam Physician. 2012 Oct 15;86(8):734-40.
PMID: 23062156BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Michael B Gill
Power Life Sciences Inc.
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CROSSOVER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 10, 2023
First Posted
February 21, 2023
Study Start
March 1, 2024
Primary Completion
March 1, 2025
Study Completion
March 1, 2026
Last Updated
June 5, 2023
Record last verified: 2023-06