Patient Guide: The Role of Circadian Factors in Regulation of Neuroplasticity in Ischemic Stroke (Observational)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 1 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
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Trial ID: NCTNCT05242393
Status: 🟢 Enrolling Now
Condition: Stroke, Ischemic, Sleep Disorder
Phase: Not Specified

Where You Can Participate

This study is available at 1 location across the country.

Top locations include:
  • • St Petersburg,

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The Role of Circadian Factors in Regulation of Neuroplasticity in Ischemic Stroke (Observational) - Join Clinical Trial NCTNCT05242393

How to Join This Clinical Trial - NCTNCT05242393

Learn how to participate in this Not Specified trial studying an investigational therapy for Stroke, Ischemic, Sleep Disorder. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Stroke, Ischemic, Sleep Disorder. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Stroke, Ischemic, Sleep Disorder
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05242393 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 1 locations. Find a study site near you:

Clinical Research Site

St Petersburg, 197341 - Russian Federation

Status: RECRUITING

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Stroke, Ischemic, Sleep Disorder:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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