Expired Study
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Richmond, Virginia 23298


Within this study patient data are collected from different imaging and motion monitoring devices that will be used to develop and test strategies for image-guided adaptive radiotherapy in cervix cancer patients.


Inclusion Criteria: - Histological diagnosis of cervix cancer - Prescription of radiation treatment to the primary cancer Exclusion Criteria: - Prior radiation treatment to the pelvis

Study is Available At:

Original ID:




Secondary ID:


Study Acronym:

Brief Title:

Image-guided Adaptive Radiotherapy for Cervix Cancer: Patient Image Acquisition

Official Title:

Image-guided Adaptive Radiotherapy for Cervix Cancer: Patient Image Acquisition

Overall Status:


Study Phase:




Minimum Age:

18 Years

Maximum Age:


Quick Facts

Healthy Volunteers
Oversight Has DMC
Study Is FDA Regulated
Study Is Section 801
Has Expanded Access

Study Source:

Virginia Commonwealth University

Oversight Authority:

United States: Institutional Review Board

Reasons Why Stopped:

Due to competing studies no further subjects

Study Type:


Study Design:

Observational Model: Cohort, Time Perspective: Pro

Number of Arms:


Number of Groups:


Total Enrollment:


Enrollment Type:


Overall Contact Information

Official Name:Jeffrey F Williamson, PhD
Principal Investigator
Virginia Commonwealth University, Department of Radiation Oncology

Study Dates

Start Date:March 2009
Completion Date:December 2013
Completion Type:Anticipated
Primary Completion Date:December 2013
Primary Completion Type:Anticipated
Verification Date:December 2013
Last Changed Date:December 19, 2013
First Received Date:December 11, 2007

Study Outcomes

Outcome Type:Primary Outcome
Measure:Increase in therapeutic ratio
Time Frame:5 years
Safety Issues:False

Study Interventions

There are no available Study Interventions

Study Arms

Study Arm Type:Other
Arm Name:cervix cancer patients

Study Agencies

Agency Class:Other
Agency Type:Lead Sponsor
Agency Name:Virginia Commonwealth University
Agency Class:NIH
Agency Type:Collaborator
Agency Name:National Cancer Institute (NCI)

Samples and Retentions

Study Population: University hospital clinic
Sample Method:Probability Sample

Study References

There are no available Study References

Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

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