Optimizing Liver MRI Using Breath-Holding With and Without Oxygen
University of California, San Francisco · NCT07135401
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–75 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 10
- US sites recruiting
- 1
- Study start
- December 1, 2025
- Record last updated
- April 13, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The goal of this interventional study (clinical trial) is to learn if different breath-holding techniques, with and without extra oxygen, can improve the quality of abdominal Magnetic Resonance Imaging (MRI) images in healthy adults, ages 18-75.
The main questions it aims to answer are
- Does breath-holding at end-expiration improve image quality in abdominal MRI scans?
- Does adding oxygen while breath-holding further reduce motion artifacts in abdominal MRI scans?
Researchers will compare breath-holding with and without oxygen to see if using oxygen improves image quality during MRI scans.
Participants will
- Be pre-screened for MRI safety and trained on breath-hold procedures
- Have one non-contrast abdominal MRI scan at the University of California San Francisco (UCSF) China Basin Imaging Center
- Use two different breath-holding techniques during the scan, with and without oxygen
- Complete one study visit lasting about 45 minutes to 1 hour
Being studied: Breath-hold conditions
Conditions: MRI; MRI Image Enhancement
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Subject must be within 18-75 years of age;
- Subject must be able to hear and understand instructions without assistive devices;
- Subject must provide written informed consent;
- Subject has the necessary mental capacity to understand instructions, and is able to comply with protocol requirements;
- Subject is able to remain still for duration of imaging procedure (approximately 30-45 minutes)
Exclusion Criteria
- Subjects with a weight greater than 499 lbs;
- Subjects that have metallic/conductive or electrically/magnetically active implants without Magnetic Resonance (MR) Safe or Magnetic Resonance (MR) Conditional labeling, with the exception of dental devices/fillings, surgical clips, and surgical staples determined to be safe for MRI scanning by a physician investigator;
- Subjects that have implants with MR Unsafe labeling;
- Subjects that have implants labeled as MR Conditional by the manufacturer for which the allowable conditions are not expected to be achieved by the MR environment or scan protocol;
- Subjects who have a contraindication to MRI per the screening policy of the participating site;
- Subjects with any respiratory or cardiovascular condition that could compromise safe breath holding;
- Subjects who are female and pregnant
Recruiting US locations
University of California, San Francisco
San Francisco, CA 94143
Site contact: Holland Stacey Stacey · 415-420-5100 · holland.stacey@ucsf.edu
Study contacts (from the official record)
- John P Roberts, MD · 415-353-3677 · John.Roberts@ucsf.edu
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