Neurologic Deficits

3

Review clinical trials related to Neurologic Deficits. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

NeuroVision vs Standard Neuromonitoring

The purpose of this study is to perform a prospective, randomized, controlled clinical trial to assess the utility of IONM in patients undergoing primary, single or multilevel lateral spinal procedures. Subjects will be randomized to undergo a lateral spine surgery with the use of NeuroVision® IONM or conventional hospital based IONM to assess incidence of new-onset neurological injury.

Participants needed: 148
Trial details
Biological sex: AllType: InterventionalSponsor: Rush University Medical CenterUpdated: Apr 7, 2026Locations: 1
Eligibility criteria

Patients undergoing a primary single or multilevel lateral spinal surgery proced... [+1]

Active infection [+2]

Status: Recruiting

Trans-Auricular Stimulation for Postoperative Inflammation in Spine Surgery

This study is a randomized controlled trial that will evaluate the effect of non-invasive auricular vagal nerve stimulation on inflammatory markers, glycemic control, postoperative pain, and inflammation-related clinical outcomes after long-segment spinal fusion surgeries when compared to current accepted management.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Alexander T. YahandaUpdated: Feb 20, 2026Locations: 1
Eligibility criteria

Long-segment spinal fusions (defined as constructs spanning at least L2-pelvis f... [+1]

Patients <18 years of age [+6]

Status: Recruiting

CARbon monoxidE intoxiCatiOn in Korea: Prospective Cohort (CARE CO Cohort)

This prospective cohort study enrolls subjects who experience carbon monoxide (CO) poisoning. The purpose of the study is to evaluate therapeutic effects of various treatments and short and long-term outcomes in CO poisoned patients. In addition, complications of brain and heart susceptible to CO are investigated through various ways and the association between complications and the patient's prognosis is also investigated. All subjects will be regularly monitored by physicians participating in this study.

Participants needed: 1,500
Trial details
Biological sex: AllType: ObservationalSponsor: Wonju Severance Christian HospitalUpdated: Jul 23, 2024Locations: 1
Eligibility criteria

Acute CO poisoning

Declined to enrollment in the study