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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01135823
Other study ID # SU-07292009-3461
Secondary ID 97085PEDSVAR0001
Status Completed
Phase N/A
First received June 1, 2010
Last updated June 2, 2010
Start date July 2006
Est. completion date June 2008

Study information

Verified date June 2010
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The primary purpose of the proposed research is to explore methods of obtaining symptom assessments from pediatric oncology patients and/or their caregivers in hopes of improving the accuracy and thoroughness of these reports. Additionally the researchers hope to simply staff efforts in obtaining detailed medical histories from pediatric oncology patients.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date June 2008
Est. primary completion date June 2008
Accepts healthy volunteers No
Gender Both
Age group N/A to 18 Years
Eligibility Inclusion Criteria:

- Approximately 150 patients ages 0-18 years (75 for each group-intervention and control) will be enrolled.

- These patients will be pediatric oncology patients who have received chemotherapy within the prior four weeks and being seen in the oncology clinic for an out-patient visit.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Intervention

Procedure:
Patient survey


Locations

Country Name City State
United States Stanford University School of Medicine Stanford California

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

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