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RECRUITING

A Study to Estimate How Often Post-stroke Spasticity Occurs and to Provide a Standard Guideline on the Best Way to Monitor Its Development

NCT06055725 · View on ClinicalTrials.gov ↗

Study Summary

This study will monitor patients during the first year following their stroke. Stroke is a very serious condition where there is a sudden interruption of blood flow in the brain. The main aim of the study will be to find out how many of those who experience their first-ever stroke then go on to develop spasticity that would benefit from treatment with medication. Spasticity is a common post-stroke condition that causes stiff or ridged muscles. The results of this study will provide a standard guideline on the best way to monitor the development of post-stroke spasticity.

Study Locations (20)

Texas

  • The University Of Texas Southwestern Medical Center — Dallas
  • McGovern Medical School - UT Physicians - Neurology (Adult Neurology Clinic) - Texas Medical Center Location — Houston
  • The University of Texas Health Science Center — San Antonio

California

  • Loma Linda — Anderson
  • University Of California, Los Angeles Medical Center — Los Angeles

Florida

  • University of South Florida (USF) - Morsani Center (USF Health Carol and Frank Morsani Center for Advanced Healthcare) — Florida City
  • Knight Neurology — Rockledge

Massachusetts

  • Massachusetts General Hospital — Boston
  • Spaulding Rehabilitation Hospital — Boston

Nebraska

  • Methodist Physicians Clinic — Omaha
  • Madonna Rehabilitation Hospital - Omaha Campus — Omaha

Georgia

  • Emory University Merge — Atlanta

Maryland

  • Medstar Health Research Institute, Inc — Hyattsville

Minnesota

  • Mayo Clinic — Rochester

Trial Details

FieldValue
Enrollment Target 1,051 participants
Start Date 2023-11-01
Est. Completion 2027-11-30

Sponsor

Ipsen

205 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06055725

The ClinicalTrials.gov registry entry for NCT06055725 describes a study currently listed as 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 1,051 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ipsen, which has 205 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 Spasticity as Sequela of Stroke appearing as the primary indexed condition, and to 0 interventions. 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: NCT06055725 reports 20 study locations spanning 14 distinct geographic areas — top geographies include Texas, California, Florida. 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 NCT06055725 about?

NCT06055725 is a clinical study titled "A Study to Estimate How Often Post-stroke Spasticity Occurs and to Provide a Standard Guideline on the Best Way to Monitor Its Development". This study will monitor patients during the first year following their stroke. Stroke is a very serious condition where there is a sudden interruption of blood flow in the brain. The main aim of the study will be to find out how many of those who experience their first-ever stroke then go on to de...

What is the current status of trial NCT06055725?

This trial is currently recruiting. The enrollment target is 1,051 participants. The study started on 2023-11-01. Estimated completion is 2027-11-30.

What conditions does trial NCT06055725 study?

This clinical trial studies the following conditions: Spasticity as Sequela of Stroke. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

Who is sponsoring clinical trial NCT06055725?

This trial is sponsored by Ipsen, which has 205 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06055725 being conducted?

This trial has 20 study locations across California, Florida, Georgia, Maryland, Massachusetts. 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