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NCT01478243 Clinical Trial

Study of Psycho-Social Impact of Keloid

Keloid Clinical Trial

Official title:
Study of Psycho-Social Impact of Keloid

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT01478243
Other study ID # 11-07
Secondary ID
Status Terminated
Phase N/A
First received November 20, 2011
Last updated October 17, 2016
Start date September 2012
Est. completion date September 2012

Study information
Verified date October 2016
Source Tirgan, Michael H., M.D.
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Despite their benign nature, keloids may constitute a severe aesthetic, and in some cases, functional problem which translates to various repercussions on person's quality of life, including much stress and insecurities.

Keloids are mostly observed between the ages of 10 and 30. Although keloid is a common condition and the investigators can make assumptions about those living with keloids, the investigators do not know the actual impact of the illness on the overall performance of patients' and how this disease, day to day, is impacting their lives. The investigators are conducting this study, aimed to investigate the psychosocial impact of keloid on daily life. Information is collected anonymously. You must be 18 years of age or older to take this survey. Parents can respond on behalf of their children who are not 18 years of age yet. The online survey will take 20-30 minutes to complete.

Recruitment information / eligibility
Status Terminated
Enrollment 1000
Est. completion date September 2012
Est. primary completion date September 2012
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

1. Clinical Diagnosis of Keloid

2. Informed consent

3. Age above 18 to answer the survey questions

4. Parents shall respond on behalf of their minor children

Study Design

Observational Model: Case-Only, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Locations
Country Name City State
United States Michael H. Tirgan MD New York New York

Sponsors (1)
Lead Sponsor Collaborator
Tirgan, Michael H., M.D.

Country where clinical trial is conducted

United States, 

See also
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Enrolling by invitation NCT05461157 - Preoperative Silicone Ointment and Wound Healing N/A
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