NCT00571415

Brief Summary

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.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
21

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Mar 2009

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 11, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

December 12, 2007

Completed
1.2 years until next milestone

Study Start

First participant enrolled

March 1, 2009

Completed
4.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2013

Completed
2.4 years until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2015

Completed
Last Updated

June 1, 2016

Status Verified

May 1, 2016

Enrollment Period

4.2 years

First QC Date

December 11, 2007

Last Update Submit

May 27, 2016

Conditions

Cervix Cancer

Keywords

Image guided adaptive radiotherapy

Outcome Measures

Primary Outcomes (1)

  • Increase in therapeutic ratio

    5 years

Study Arms (1)

cervix cancer patients

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

University hospital clinic

You may qualify if:

  • Histological diagnosis of cervix cancer
  • Prescription of radiation treatment to the primary cancer

You may not qualify if:

  • Prior radiation treatment to the pelvis

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Viriginia Commonwealth University, Department of Radiation Oncology

Richmond, Virginia, 23298, United States

Location

MeSH Terms

Conditions

Uterine Cervical Neoplasms

Condition Hierarchy (Ancestors)

Uterine NeoplasmsGenital Neoplasms, FemaleUrogenital NeoplasmsNeoplasms by SiteNeoplasmsUterine Cervical DiseasesUterine DiseasesGenital Diseases, FemaleFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesGenital Diseases

Study Officials

  • Jeffrey F Williamson, PhD

    Virginia Commonwealth University, Department of Radiation Oncology

    PRINCIPAL INVESTIGATOR

  • Jeffrey F Williamson, PhD

    VCU, Richmond, VA

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 11, 2007

First Posted

December 12, 2007

Study Start

March 1, 2009

Primary Completion

May 1, 2013

Study Completion

October 1, 2015

Last Updated

June 1, 2016

Record last verified: 2016-05

Locations

US(1)