Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06975072 · ClinicalTrials.gov registry record · Phase 4

Effect of Magnesium on Neuromonitoring

A Phase 4 study of Pain and Spine Fusion, sponsored by University of California, San Francisco.

Recruiting
Registry status
Phase 4
Development phase
20
Enrollment target
1
Study location

NCT06975072: Recruiting Phase 4 study of Pain and Spine Fusion, sponsored by University of California, San Francisco.

NCT06975072 is a Phase 4 study of Pain and Spine Fusion that is actively recruiting participants, run by University of California, San Francisco. The registered enrollment target is 20 participants, below the 304-participant average among 374 other Pain trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06975072, a Phase 4 study of Pain and Spine Fusion, is actively recruiting participants, sponsored by University of California, San Francisco.

RECRUITING
Registry status
Phase 4
Development phase
20 participants
Enrollment target
1
Study location

Study Summary

Intraoperative neurophysiologic monitoring (IONM) is commonly used during complex spinal surgery to monitor the integrity of neural structures and improve the perioperative safety profile. Transcranial Motor Evoked Potentials (TcMEPs) monitor the integrity of the motor pathways and are one of the most commonly used monitoring modalities in spinal surgery. Because inhaled anesthetics can negatively affect the ability to monitor TcMEPs, anesthesiologists commonly use a combination of propofol and opioids to maintain the anesthetic state. Additionally, anesthesiologists will frequently administer intravenous infusions of medications that can decrease postoperative pain and opioid use (called opioid-sparing adjuncts) because spinal surgeries result in significant postoperative pain. Despite the increasing use of these agents, there is scant clinical data about how they may affect the integrity of TcMEP monitoring. Magnesium (Mg), a N-methyl-d-aspartate receptors (NMDA) receptor antagonist, is one of the adjuncts with robust data supporting clinical efficacy to decrease pain and opioid use on TcMEPs. Mg has been used clinically for decades. The investigators commonly utilize intravenous magnesium as a component of our spinal anesthesia protocol. However, there is only a single case report that discusses the effects of Mg on TcMEPs. Here the investigators propose a prospective clinical trial to quantitatively assess the effects of various Mg plasma levels on TcMEPs. There is a lack of literature on the pharmacokinetics of magnesium in non-pregnant patients.

Primary Outcome

Serum magnesium level will be measured by UCSF Lab.

Interventions

  • DRUG Magnesium sulfate administration

Study Locations (1)

California

  • University of California San Francisco Hospital - San Francisco

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2025-07-01
Est. Completion 2026-04-30
Phase Phase 4

What NCT06975072 shows while recruiting

NCT06975072 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 304-participant average among 374 other Pain trials with a reported enrollment target (93% lower).

The record links to 6 conditions, with Pain appearing as the primary indexed condition, and to 1 intervention - of which Magnesium sulfate administration is the first listed.

NCT06975072 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT06975072 about?

NCT06975072 is a clinical study titled "Effect of Magnesium on Neuromonitoring". Intraoperative neurophysiologic monitoring (IONM) is commonly used during complex spinal surgery to monitor the integrity of neural structures and improve the perioperative safety profile. Transcranial Motor Evoked Potentials (TcMEPs) monitor the integrity of the motor pathways and are one of the mo...

What is the current status of trial NCT06975072?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 20 participants. The study started on 2025-07-01. Estimated completion is 2026-04-30.

What conditions does trial NCT06975072 study?

This clinical trial studies the following conditions: Pain, Spine Fusion, Spine Surgery, Spine, Spine Surgery With Neuromonitoring.

What interventions are being tested in trial NCT06975072?

The interventions under investigation include: Magnesium sulfate administration (DRUG).

Who is sponsoring clinical trial NCT06975072?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06975072 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Pain

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06975072's enrollment target sits among peer trials

20 338th of 374 higher than 29 of 374 other Pain trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Pain trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00573339 · 20 participants

    Cardiac Magnetic Resonance Imaging (MRI) Normal Reference Control Group Testing

  • NCT00692939 · 20 participants · Phase 1

    Autologous Stem Cell Transplantation for Crohn's Disease

  • NCT00967785 · 20 participants · Phase 1

    A Phase I Study of Mozobil in the Treatment of Patients With WHIMS

  • NCT01406691 · 20 participants · Phase 4

    Light Flashes to Treat Delayed Sleep Phase Disorder (DSPD)

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06975072, the US trial registry maintained by the National Library of Medicine. NCT06975072 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.