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Trigeminal Evoked Responses to Improve Rhizotomy

Trigeminal Evoked Responses to Improve Rhizotomy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05738096
Enrollment
30
Registered
2023-02-21
Start date
2023-11-01
Completion date
2026-11-01
Last updated
2025-11-26

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

Conditions

Rhizotomy, Trigeminal Neuralgia

Brief summary

Trigeminal neuralgia (TGN) is a debilitating pain syndrome where electrical, shock- like jolts of pain affect the face. Trigeminal somatosensory evoked potentials (TSEPs) provide a promising modality for measuring the trigeminal sensory and nociceptive pathway by using peripheral stimulation of the trigeminal nerve (on the skin) and measuring low latency evoked potentials on the scalp (contralateral sensory cortex). While TSEPs have been measured in the past, it is not clear if implementing TSEPs into a routine neurosurgical rhizotomy procedure will be feasible. This is a prospective cohort study examining the feasibility of routinely performing TSEPs during rhizotomies for TGN.

Interventions

OTHERTSEP + rhizotomy surgery

TGN patients recruited for this study will already be undergoing percutaneous rhizotomy surgery. TSEPs will be measured at baseline prior to surgery. During the rhizotomy procedure, an electrode or balloon is placed through a metal sheath to then damage the nerve. A stylet is introduced to clear tissue from the sheath in preparation for the electrode or balloon. Prior to the final insertion of the RF electrode where the gasserian ganglion will be damaged, we will place a standard stereotactic EEG electrode (SEEG). Following damaging the nerve (clinical procedure), we will record again to measure differences in the TSEPs following cell body damage. The Neuralynx system will be used to record the potentials at 40 KHz.

OTHERTSEPs recording only

TSEPS will also be recorded from healthy controls in a lab setting; all procedures for the healthy controls will be non-invasive.

Sponsors

University of Minnesota
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* Adults of 18 years or older * Scheduled to undergo percutaneous rhizotomy for facial pain

Exclusion criteria

* For TGN: Facial pain of unclear origin (i.e. not clearly TGN pain) or Rhizotomy procedure canceled * For Healthy control: Diagnosis or history of facial pain such as TMD or TGN, History of migraine, History of any functional pain disorder: fibromyalgia, IBS, CRPS or Recent chronic pain (within last month)

Design outcomes

Primary

MeasureTime frameDescription
Feasibility3 yearstotal study procedure completion rate

Secondary

MeasureTime frameDescription
TSEPS latency within TGN1 daydifference in measured TSEPS latency between normal and TGN side
TSEPS peak to peak amplitude within TGN1 daydifference in measured peak to peak amplitude between normal and TGN side
TSEPS peak to peak amplitude between control and TGN patients1 daydifference in measured peak to peak amplitude between healthy participants and TGN patients
TSEPS latency between control and TGN patients1 daydifference in latency between healthy participants and TGN patients

Countries

United States

Contacts

Primary ContactMatthew Maple
maple036@umn.edu612-626-3582

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026