NCT01661062

Brief Summary

Cone beam CT (computed tomography) is a developing technology which allows CT images to be obtained while a patient is on the radiation treatment table.(A CT scan uses x-rays to produce detailed pictures of structures in the body.) In this study, cone beam CT scans will be obtained before individual radiation treatment sessions for head and neck cancer. The information gathered from these scans will be used by the researchers to look at patient movement as well as changes in the amount of normal and tumor tissue throughout the course of radiation therapy. The researchers will use this information to create hypothetical radiation treatment plans, which will be used as the basis for future research. The cone beam CT scan data will not be used to alter the actual radiation treatment of any of the patients enrolled on the study. In addition, tests of salivary output and swallowing and questionnaires about quality of life will be made to assess how the doses of radiation affect them.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
23

participants targeted

Target at below P25 for not_applicable head-and-neck-cancer

Timeline
Completed

Started Jan 2009

Longer than P75 for not_applicable head-and-neck-cancer

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

January 1, 2009

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2011

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

September 26, 2011

Completed
11 months until next milestone

First Posted

Study publicly available on registry

August 9, 2012

Completed
2.2 years until next milestone

Results Posted

Study results publicly available

October 31, 2014

Completed
1.3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2016

Completed
Last Updated

August 29, 2016

Status Verified

July 1, 2016

Enrollment Period

2.2 years

First QC Date

September 26, 2011

Results QC Date

October 21, 2014

Last Update Submit

July 26, 2016

Conditions

Outcome Measures

Primary Outcomes (2)

  • Rate of Movement of Normal Tissue

    The primary outcome measure of this study is to characterize patient-specific target and normal tissue movement.

    approximately 7 weeks

  • Correlation Coefficient for the Association Between Delivered Mean Parotid Dose and Salivary Flow Rate

    Spearman rank-based correlation coefficients were calculated for the association between saliva flow rate and the delivered mean parotid doses at several timepoints (Baseline, 3 months, 6 months, 12 months, 18 months, and 24 months).

    24 months

Secondary Outcomes (2)

  • Improvement of Image Quality

    36 months

  • The Median Delivered Dose of Radiation to the Parotid Gland

    7 weeks

Study Arms (1)

Cone Beam CT

EXPERIMENTAL

All patients will be included in the treatment arm of this study. For the purposes of this study patients will get CT scans every day for the length of their radiation therapy (in order to assess if CT every day provides additional information compared with CT scans performed less frequently). Although the exact amount of radiation patients get will be determined by their doctor, it is expected that they will get approximately 7 weeks, approximately 35 total cone beam CT scans.

Other: Cone Beam Computed Tomography (CT) Scan

Interventions

Cone beam CT scan is considered a noninvasive procedure (meaning that the procedure does not require breaking the skin or any tools that physically enter the body). It will add a small amount of additional radiation dose (less than 1%) to the head and neck. The increase in the amount of radiation is only a very small amount more than what patients who get standard daily imaging receive. The amount of radiation from the cone beam CT scans is not significant (less than 1%) when compared to the amount of radiation generally received for treatment of head and neck cancer.

Also known as: CBCT
Cone Beam CT

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients of all ages ≥18, both sexes, and all races will be included in this study. Pregnant females will be excluded. No other special classes of subjects (i.e., prisoners) will be entered.
  • Patients must be diagnosed with biopsy-proven squamous cell carcinoma of the head and neck.
  • Patients must be recommended treatment with definitive radiation therapy with concurrent chemotherapy, but without prior surgical resection of the primary tumor or lymph nodes
  • Patients must be recommended a treatment course of at least 30 radiation fractions
  • Patients must sign an informed consent form approved for this purpose by the Institutional Review Board (IRB) of the University of Michigan Hospital indicating that they are aware that undergoing cone beam CT of the head and neck is voluntary and has potential risks.

You may not qualify if:

  • Patients must not have a history of prior radiation to the head or neck

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Michigan Comprehensive Cancer Center

Ann Arbor, Michigan, 48109, United States

Location

Related Publications (1)

  • Hunter KU, Fernandes LL, Vineberg KA, McShan D, Antonuk AE, Cornwall C, Feng M, Schipper MJ, Balter JM, Eisbruch A. Parotid glands dose-effect relationships based on their actually delivered doses: implications for adaptive replanning in radiation therapy of head-and-neck cancer. Int J Radiat Oncol Biol Phys. 2013 Nov 15;87(4):676-82. doi: 10.1016/j.ijrobp.2013.07.040. Epub 2013 Sep 10.

MeSH Terms

Conditions

Head and Neck Neoplasms

Condition Hierarchy (Ancestors)

Neoplasms by SiteNeoplasms

Results Point of Contact

Title
Avraham Eisbruch, M.D.
Organization
University of Michigan Comprehensive Cancer Center

Study Officials

  • Avraham Eisbruch, MD

    University of Michigan Rogel Cancer Center

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 26, 2011

First Posted

August 9, 2012

Study Start

January 1, 2009

Primary Completion

March 1, 2011

Study Completion

March 1, 2016

Last Updated

August 29, 2016

Results First Posted

October 31, 2014

Record last verified: 2016-07

Locations