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Spots Global Cancer Trial Database for Registration and Informed Consent Study for the Childhood Cancer Research Network

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Registration and Informed Consent Study for the Childhood Cancer Research Network

Official Title: Protocol for Registration and Consent to the Childhood Cancer Research Network - A Limited Institution Pilot

Study ID: NCT00433394

Study Description

Brief Summary: RATIONALE: Collecting informed consent from parents of children with cancer to register with the Childhood Cancer Research Network may help the study of cancer in the future. PURPOSE: This study is collecting informed consent to register younger patients with cancer into the Childhood Cancer Research Network.

Detailed Description: OBJECTIVES: * Obtain informed consent from parents (and the child, when appropriate) of children diagnosed with cancer (who are under 21 years of age) to register their child's name and address with the Childhood Cancer Research Network. * Obtain informed consent from parents (and the child, when appropriate) of children diagnosed with cancer (who are under 21 years of age) to be contacted in the future for possible participation in non-therapeutic research studies involving the parents and/or child. * Facilitate the systematic registration of pediatric and adolescent patients diagnosed with cancer into the Childhood Cancer Research Network. OUTLINE: Consent is obtained from parents (and pediatric patients, where applicable) to register the patient's and parent's names and addresses with the Childhood Cancer Research Network, provide a copy of the pathology report to the Network, and contact parents in the future for possible non-therapeutic research studies involving the parents and/or child. Information provided will be held in strict confidence. PROJECTED ACCRUAL: Not specified

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Jonathan Jaques Children's Cancer Center at Miller Children's Hospital, Long Beach, California, United States

Carole and Ray Neag Comprehensive Cancer Center at the University of Connecticut Health Center, Farmington, Connecticut, United States

Lee Cancer Care of Lee Memorial Health System, Fort Myers, Florida, United States

University of Florida Shands Cancer Center, Gainesville, Florida, United States

Cancer Research Center of Hawaii, Honolulu, Hawaii, United States

Advocate Lutheran General Cancer Care Center, Park Ridge, Illinois, United States

Breslin Cancer Center at Ingham Regional Medical Center, Lansing, Michigan, United States

Children's Hospitals and Clinics of Minneapolis, Minneapolis, Minnesota, United States

Norris Cotton Cancer Center at Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, United States

Hackensack University Medical Center Cancer Center, Hackensack, New Jersey, United States

Albany Medical Center Hospital, Albany, New York, United States

NYU Cancer Institute at New York University Medical Center, New York, New York, United States

Mission Hospitals - Memorial Campus, Asheville, North Carolina, United States

Children's Medical Center - Dayton, Dayton, Ohio, United States

Tod Children's Hospital - Forum Health, Youngstown, Ohio, United States

St. Christopher's Hospital for Children, Philadelphia, Pennsylvania, United States

East Tennessee Children's Hospital, Knoxville, Tennessee, United States

Driscoll Children's Hospital, Corpus Christi, Texas, United States

Fletcher Allen Health Care - University Health Center Campus, Burlington, Vermont, United States

University of Alberta Hospital, Edmonton, Alberta, Canada

Montreal Children's Hospital at McGill University Health Center, Montreal, Quebec, Canada

Contact Details

Name: Julie A. Ross, PhD

Affiliation: Masonic Cancer Center, University of Minnesota

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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