Breathing Cycle Biofeedback During Computed Tomography Procedures
Respiratory Cycle Biofeedback During CT Guided Procedures
2 other identifiers
observational
30
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Apr 2003
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2003
CompletedFirst Submitted
Initial submission to the registry
April 18, 2003
CompletedFirst Posted
Study publicly available on registry
April 18, 2003
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2006
CompletedMarch 4, 2008
March 1, 2006
April 18, 2003
March 3, 2008
Conditions
Keywords
Eligibility Criteria
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
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: 11110962BACKGROUNDFrohlich 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: 4001413BACKGROUNDConnolly 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