NCT00059137

Brief Summary

This study will evaluate the effectiveness of a flexible belt device in guiding patient breathing during computed tomography (CT)-guided needle biopsy. When patients undergo CT scanning to help guide the physician during a tissue biopsy, they are usually asked to hold their breath while the scan is taken of certain parts of the body. When the first scan is completed, the patients are allowed to breathe, and are then asked to hold their breath again while the needle is advanced towards the tissue to be biopsied. Since body organs and tissues move with breathing, this study will try to stop the patient's breathing at the same place in the breathing cycle to ensure that the biopsy target stays still and in the same place. This study will see if the flexible belt, used with a computer screen that charts the patient's breathing, will improve the patient's ability to stop breathing at the same place in the breathing cycle before and during the biopsy. Patients 18 years of age and older who have a lesion requiring a needle biopsy in the chest or abdominal area may be eligible for this study. The biopsy procedure must require CT scan guidance. Participants will undergo the following procedures:

  • Breathing exercise: A flexible, loose-fitting belt is placed around the patient's abdomen and the patient is asked to stop breathing in the following ways: 1) take a deep breath in and hold; 2) breathe deeply out and hold; and 3) breathe regularly and hold.
  • Needle biopsy: The patient is positioned in a CT scanner and is asked to hold his or her breath while an initial scan is taken. Then the patient is taken out of the scanner and the place the needle entry site for the biopsy is marked on the skin. A local anesthetic is applied to the site and the patient is asked to hold his or her breath the same way as before. During this breath hold, the patient may or may not be shown a computer screen displaying a graph of the patient's breathing and the point in the cycle of the previous breath hold. The biopsy is then performed with CT guidance. While the CT pictures are being taken, the patient is again asked to breathe and hold his or her breath as before. When the biopsy is completed, the belt device is removed.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Apr 2003

Typical duration for all trials

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

April 1, 2003

Completed
17 days until next milestone

First Submitted

Initial submission to the registry

April 18, 2003

Completed
Same day until next milestone

First Posted

Study publicly available on registry

April 18, 2003

Completed
2.9 years until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2006

Completed
Last Updated

March 4, 2008

Status Verified

March 1, 2006

First QC Date

April 18, 2003

Last Update Submit

March 3, 2008

Conditions

Keywords

GatingRespiratory MisregistrationAbdominal BeltPercutaneousCT Guided BiopsyRespiratory CycleNeedle Biopsy

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Patients must fulfill all of the following criteria to be eligible for study admission:
  • All patients must have a lesion needing biopsy in the chest or abdominal areas in special procedures requiring CT scan guidance.
  • age greater than 18 years.
  • No serious concurrent medical illness that would preclude the patient from making a rational informed decision on participation.
  • The ability to understand and willingness to sign a written informed consent form, and to comply with the protocol. If in question, an ethics consult will be obtained.

You may not qualify if:

  • Patients with any of the following will be excluded from study entry:
  • Patients with an altered mental status that precludes understanding or consenting for the biopsy procedure will be excluded from this study.
  • patients unable to hold breath for more than 5 seconds.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Institutes of Health Clinical Center (CC)

Bethesda, Maryland, 20892, United States

Location

Related Publications (3)

  • Tomiyama N, Mihara N, Maeda M, Johkoh T, Kozuka T, Honda O, Hamada S, Yoshida S, Nakamura H. CT-guided needle biopsy of small pulmonary nodules: value of respiratory gating. Radiology. 2000 Dec;217(3):907-10. doi: 10.1148/radiology.217.3.r00dc10907.

    PMID: 11110962BACKGROUND
  • Frohlich H, Dohring W. A simple device for breath-level monitoring during CT. Radiology. 1985 Jul;156(1):235. doi: 10.1148/radiology.156.1.4001413.

    PMID: 4001413BACKGROUND
  • Connolly BL, Chait PG, Duncan DS, Taylor G. CT-guided percutaneous needle biopsy of small lung nodules in children. Pediatr Radiol. 1999 May;29(5):342-6. doi: 10.1007/s002470050603.

    PMID: 10382211BACKGROUND

Study Design

Study Type
observational
Sponsor Type
NIH

Study Record Dates

First Submitted

April 18, 2003

First Posted

April 18, 2003

Study Start

April 1, 2003

Study Completion

March 1, 2006

Last Updated

March 4, 2008

Record last verified: 2006-03

Locations