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ACTIVE NOT RECRUITING

Cerebral Hemodynamics and Microemboli During Placement of Relay®Branch Thoracic Stent-Graft System

NCT05155956 · View on ClinicalTrials.gov ↗

Study Summary

This is an observational cohort study addressing the incidence of cerebral microemboli and alterations of cerebral hemodynamic physiology of the Relay®Branch thoracic stent-graft system.

Interventions

  • OTHER transcranial Doppler ultrasonography (TCD)

Study Locations (2)

Pennsylvania

  • Hospital of the University of Pennsylvania — Philadelphia
  • Penn Presbyterian Medical Center — Philadelphia

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2021-12-15
Est. Completion 2026-12

Sponsor

University of Pennsylvania

1,457 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05155956

The ClinicalTrials.gov registry entry for NCT05155956 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, 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 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Pennsylvania, which has 1,457 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Thoracic Aortic Aneurysm appearing as the primary indexed condition, and to 1 intervention — of which transcranial Doppler ultrasonography (TCD) 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: NCT05155956 reports 2 study locations spanning 1 distinct geographic area — top geographies include Pennsylvania. 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 NCT05155956 about?

NCT05155956 is a clinical study titled "Cerebral Hemodynamics and Microemboli During Placement of Relay®Branch Thoracic Stent-Graft System". This is an observational cohort study addressing the incidence of cerebral microemboli and alterations of cerebral hemodynamic physiology of the Relay®Branch thoracic stent-graft system.

What is the current status of trial NCT05155956?

This trial is currently active not recruiting. The enrollment target is 20 participants. The study started on 2021-12-15. Estimated completion is 2026-12.

What conditions does trial NCT05155956 study?

This clinical trial studies the following conditions: Thoracic Aortic Aneurysm, Thoracic Aortic Dissection, Microemboli. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05155956?

The interventions under investigation include: transcranial Doppler ultrasonography (TCD) (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05155956?

This trial is sponsored by University of Pennsylvania, which has 1,457 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05155956 being conducted?

This trial has 2 study locations across Pennsylvania. 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