Clinical trial Recruiting at 1 site Observational Ages 18 to 75

3D MRI Elastography to Peek at Vestibular Schwannoma Stiffness and How It Relates to Surgery

Official title: Evaluation of Vestibular Schwannoma Mechanical Properties and Histological Features Using Three-Dimensional Magnetic Resonance Elastography

Run by Shengjing Hospital · NCT07844460 · Data updated 2026-11-12

This study tests whether 3D MRI elastography can noninvasively measure how stiff vestibular schwannomas are and how firmly they stick to nearby tissues, to help predict surgical difficulty and outcomes.

More Vestibular Schwannoma trials

Quick facts

Study typeObservational
Ages18 Years to 75 Years
SexAll
Enrollment30 (estimated)
SponsorShengjing Hospital
Academic / other
Locations1 site (Shenyang, Liaoning)
StatusRecruiting
StartedSeptember 25, 2025
Main results expectedDecember 2026
Study endsMarch 2027
Registry record updatedOctober 16, 2026
Trial IDNCT07844460 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with radiologically confirmed vestibular schwannomas scheduled for surgical resection at Shengjing Hospital who can tolerate MRI/MRE and provide informed consent.

Probably not a fit

Patients with tumors or conditions where MRE is unsafe or inconclusive, or those not undergoing planned resection, may not benefit from the imaging biomarker findings.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective, single-center study evaluates the feasibility and clinical value of three-dimensional magnetic resonance elastography (3D MRE) for preoperative assessment of vestibular schwannomas. Researchers will compare MRE-derived stiffness and adhesion maps with intraoperative observations and tumor histology, and will follow facial nerve function postoperatively to see if MRE findings relate to prognosis. Approximately 30 patients undergoing planned surgical resection will be enrolled. The goal is to determine if MRE can serve as a noninvasive biomarker to aid risk stratification, surgical planning, and patient counseling. Interventions are observational in nature, focusing on imaging correlations rather than treatment modification.

Why it matters

Potential benefit: If successful, patients could gain improved preoperative planning and counseling based on a noninvasive map of tumor stiffness and adhesion.

How similar studies have gone: Prior imaging studies have explored MRE in brain tumors; this study advances a single-center feasibility and correlation analysis specific to vestibular schwannomas.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

-All patients undergoing vestibular schwannoma resection surgery are eligible for inclusion in the study cohort.

Exclusion Criteria:

* Patients with metallic implants or foreign bodies in their bodies (pacemakers, artificial metallic heart valves, metal joints, metal implants, and those who can not remove dentures, insulin pumps, or contraceptive rings)
* Pregnant women in the first trimester (within three months)
* Patients with severe claustrophobia or anxiety
* Patients with severe fever
* Patients who can not tolerate MRE
* Patients with vascular malformations and aneurysms.
* Patients who do not sign an informed consent

Where it's running

  • Shengjing hospital
    Shenyang, Liaoning, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.