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Recruiting NCT07113353

NCT07113353 Non-Invasive ICP Monitoring Study

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Clinical Trial Summary
NCT ID NCT07113353
Status Recruiting
Phase
Sponsor University of Texas Southwestern Medical Center
Condition Intracranial Pressure
Study Type OBSERVATIONAL
Enrollment 30 participants
Start Date 2026-04-10
Primary Completion 2026-10-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Brain4Care

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 30 participants in total. It began in 2026-04-10 with a primary completion date of 2026-10-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Measuring the pressure inside the skull, which is called intracranial pressure, is important to treat severe neurological illness. Currently, measuring intracranial pressure requires doctors to place an invasive pressure monitor. Recently, a non-invasive intracranial pressure monitor has been developed. This monitor has a tiny pin that is placed on the head which measures the tiny movements of the skull every time the heart beats. This produces a waveform that looks very similar to an invasive intracranial pressure waveform. However, we don't know enough about how the non-invasive device to make it clinically useful yet.

Eligibility Criteria

Inclusion Criteria: * Adult patients (age \>18) undergoing craniotomy for any indication requiring hyperosmolar agents as a part of their surgery * Adult patients (age \>18) in the neuro-oncology or neurosurgery clinic who are receiving diagnostic/therapeutic lumbar puncture as a part of their ordinary care * Adult patients (age \>18) in the neurosurgery clinic with ventriculo-peritoneal shunts who require adjustments to increase or decrease drainage of cerebrospinal fluid. Exclusion Criteria: * Age \<18 * Lacking capacity to provide informed consent on their own behalf

Contact & Investigator

Central Contact

Noah Jouett, DO, PhD

✉ noah.jouett@utsouthwestern.edu

📞 214-633-3911

Frequently Asked Questions

Who can join the NCT07113353 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Intracranial Pressure. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07113353 currently recruiting?

Yes, NCT07113353 is actively recruiting participants. Contact the research team at noah.jouett@utsouthwestern.edu for enrollment information.

Where is the NCT07113353 trial being conducted?

This trial is being conducted at Coppell, United States.

Who is sponsoring the NCT07113353 clinical trial?

NCT07113353 is sponsored by University of Texas Southwestern Medical Center. The trial plans to enroll 30 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology