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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00601744
Other study ID # 2007-0584
Secondary ID
Status Completed
Phase N/A
First received January 15, 2008
Last updated January 9, 2013
Start date January 2008
Est. completion date January 2013

Study information

Verified date January 2013
Source M.D. Anderson Cancer Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The goal of this research study is to learn about the social and emotional factors that may affect the quality of life of patients with cancer of the eye or eye area who have had their facial appearance changed due to an orbital exenteration.


Description:

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Study Design

Observational Model: Family-Based, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Behavioral:
Audio-Taped Interview
Meeting with a research staff member either in person or by phone, lasting 2 to 2 1/2 hours Arm 1: Questions about emotional well-being, appearance, coping ability with the cancer, and the types of social relations and support available (such as relationships with friends and family) Arm 2: Questions regarding if and how social relations may have been affected by his/her cancer experiences after the orbital exenteration.
Questionnaire
5-10 minute questionnaire to be completed after the interview.

Locations

Country Name City State
United States UT MD Anderson Cancer Center Houston Texas

Sponsors (1)

Lead Sponsor Collaborator
M.D. Anderson Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary List of physical adaptation and social-psychological issues cancer patients who survive and suffer from changes in normal facial appearance as a result of orbital exenteration Participants evaluated at one time point (Interview - Questionnaire) No
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