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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02769546
Other study ID # UPCC 28815
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date January 2016
Est. completion date January 2018

Study information

Verified date April 2020
Source Abramson Cancer Center of the University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The primary objective is to administer a cross-sectional survey to directly compare the differences patients and physicians hold regarding ovarian cancer prognosis and survival, complications arising from treatment, and counseling on advance directives, living wills, palliative care, and hospice services. Overall, the project will pinpoint opportunities for better patient physician communication regarding prognosis and end-of-life care and allow for more informed and tailored decision-making.


Recruitment information / eligibility

Status Terminated
Enrollment 50
Est. completion date January 2018
Est. primary completion date January 2018
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- women over 18 years old with biopsy-confirmed malignancy

- being actively treated or are in surveillance for epithelial ovarian cancer

- have an existing therapeutic relationship with a provider who is participating in the study.

Exclusion Criteria:

- patients enrolled in palliative or hospice care programs, patients with a second primary malignancy within the last five years (excluding non-melanoma skin cancer)

- patients who are illiterate or non-English speaking, and patients without decision-making capacity.

- There are no exclusion criteria based on age, gender, economic status or race/ethnicity

Study Design


Intervention

Other:
Surveys


Locations

Country Name City State
United States Abramson Cancer Center of the University of Pennsylvania Philadelphia Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Abramson Cancer Center of the University of Pennsylvania

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of completed surveys and phone interviews 1 year
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