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Illness Related Distress in Women With Clinically Localized Cutaneous Melanoma


N/A
18 Years
N/A
Open (Enrolling)
Female
Melanoma

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Trial Information

Illness Related Distress in Women With Clinically Localized Cutaneous Melanoma


Inclusion Criteria:



- Age 18 years or older

- Clinically node-negative primary cutaneous melanoma.

- Patients participating must be female

- Patients must have completed surgical treatment for melanoma at least 10 days ago and
less than 2 years at the time of study entry.

Exclusion Criteria:

- Prior history of cancer with the exception of squamous or basal cell carcinoma of the
skin.

Type of Study:

Observational

Study Design:

Observational Model: Cohort, Time Perspective: Prospective

Outcome Measure:

To measure illness related distress regarding survival, family planning and functioning, and aesthetic satisfaction and QOL in post-surgical female patients diagnosed with clinically localized primary cutaneous melanoma.

Outcome Time Frame:

conclusion of study

Safety Issue:

No

Principal Investigator

Mary Sue Brady, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Memorial Sloan-Kettering Cancer Center

Authority:

United States: Institutional Review Board

Study ID:

08-096

NCT ID:

NCT00745862

Start Date:

August 2008

Completion Date:

August 2013

Related Keywords:

  • Melanoma
  • Skin
  • Melanoma
  • Skin Neoplasms

Name

Location
Memorial Sloan-Kettering Cancer Center New York, New York  10021