Skip to content

MRI and Local Anesthesia

MRI Evaluation of Local Anesthesia Administration

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07602686
Acronym
MRI and LA
Enrollment
102
Registered
2026-05-22
Start date
2026-12-15
Completion date
2029-07-01
Last updated
2026-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Anesthesia

Brief summary

The purpose of this research is to investigate the utility of using dental-dedicated MRI as a measurement tool to observe and evaluate the administration of local anesthesia in dental patients.

Interventions

DEVICEddMRI

Dental MRI imaging

Sponsors

University of Minnesota
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult age 18 or older * Health status of American Society of Anesthesiologists (ASA) class 1 or 2 * Able to provide informed consent * Able to appear in person at OMRIC on the days indicated for the study

Exclusion criteria

* ASA class 3 or higher * Pregnant patients * Taking any medication that would affect pain perception or interact with local anesthetic * Allergic/history of adverse reaction to local anesthetic or any component in the local anesthetic * Paresthesia in the area of innervation of Cranial Nerve V3 * Active infection or abscess in the oral and maxillofacial region * History of temporomandibular disorder, maximum incisal opening less than 15mm * History of recent dental trauma (within the past 6 months) * Dental hypersensitivity * Claustrophobia and/or conditions of anxiety or motion disorder (for MRI purposes) * Metallic, electronic, or magnetic implants or devices classified as MR Unsafe or Conditional by the American College of Radiology * Unable to give informed consent

Design outcomes

Primary

MeasureTime frameDescription
Patient reported sensation - 5min5 minutes after the nerve blockMinimum value: No numbness Maximum value: Numb High scores mean a successful outcome for the block.
Patient reported sensation - 1 hourwithin 1 hour of the nerve blockMinimum value: No numbness Maximum value: Numb High scores mean a successful outcome for the block.
Ability to sense light touchwithin 1 hour of the nerve blockbinary scale. Options are yes or no
Ability to sense pressurewithin 1 hour of the nerve blockMinimum value: 1.65 Maximum value: 6.65 Low scores mean that the participant can sense more, and that the block was less effective
Ability to sense direction of touch (only if can sense VonFrey fibers)within 1 hour of the nerve blockPatient reports direction of sensation (up/down/right/left). This is scored 5 times per site
Ability to distinguish sharp versus dull (only if can sense VonFrey fibers)within 1 hour of the nerve blockPatient reports sharp versus dull sensation. This is scored 5 times per site

Countries

United States

Contacts

CONTACTRachel Uppgaard, DDS, FACS
uppg0003@umn.edu612-209-9176
PRINCIPAL_INVESTIGATORRachel Uppgaard, DDS, FACS

University of Minnesota

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 11, 2026