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ACTIVE NOT RECRUITING NA

Evaluating Raised Intracranial Pressure Using MR Elastography

NCT03096743 · View on ClinicalTrials.gov ↗

Study Summary

Investigators will compare magnetic resonance (MR) elastography measurements to other forms of noninvasive methods of detecting raised intracranial pressure, including optical coherence tomography (OCT) imaging measurements of the retinal nerve fiber layer (RNFL) and indirect signs of raised intracranial pressure on magnetic resonance imaging (MRI).

Interventions

  • DIAGNOSTIC_TEST MR elastography
  • DIAGNOSTIC_TEST MRI structural brain imaging
  • PROCEDURE Lumbar puncture
  • DIAGNOSTIC_TEST Optical Coherence Tomography (OCT) imaging
  • DIAGNOSTIC_TEST Optic nerve B-scan ultrasound

Study Locations (1)

Minnesota

  • Mayo Clinic in Rochester — Rochester

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2017-01-10
Est. Completion 2031-12-31
Phase NA

Sponsor

Mayo Clinic

3,246 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03096743

The ClinicalTrials.gov registry entry for NCT03096743 describes a study currently listed as active not recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Mayo Clinic, which has 3,246 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Idiopathic Intracranial Hypertension appearing as the primary indexed condition, and to 5 interventions — of which MR elastography is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03096743 reports 1 study location spanning 1 distinct geographic area — top geographies include Minnesota. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03096743 about?

NCT03096743 is a clinical study titled "Evaluating Raised Intracranial Pressure Using MR Elastography". Investigators will compare magnetic resonance (MR) elastography measurements to other forms of noninvasive methods of detecting raised intracranial pressure, including optical coherence tomography (OCT) imaging measurements of the retinal nerve fiber layer (RNFL) and indirect signs of raised intracr...

What is the current status of trial NCT03096743?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 200 participants. The study started on 2017-01-10. Estimated completion is 2031-12-31.

What conditions does trial NCT03096743 study?

This clinical trial studies the following conditions: Idiopathic Intracranial Hypertension. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03096743?

The interventions under investigation include: MR elastography (DIAGNOSTIC_TEST), MRI structural brain imaging (DIAGNOSTIC_TEST), Lumbar puncture (PROCEDURE), Optical Coherence Tomography (OCT) imaging (DIAGNOSTIC_TEST), Optic nerve B-scan ultrasound (DIAGNOSTIC_TEST). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03096743?

This trial is sponsored by Mayo Clinic, which has 3,246 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03096743 being conducted?

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

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial