Patient Guide: Observational Study of Patients With Moderate to Severe Chronic Plaque Psoriasis

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 302 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT03982394
Status: ACTIVE_NOT_RECRUITING
Condition: Chronic Plaque Psoriasis
Phase: Research Study

Where You Can Participate

This study is available at 302 locations across the country.

Top locations include:
  • • Lomas de Zamora, Buenos Aires
  • • Pilar, Buenos Aires
  • • Ciudad Autonoma Buenos Aires, Ciudad Autonoma De Buenos Aires
  • • And 299 more locations

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Observational Study of Patients With Moderate to Severe Chronic Plaque Psoriasis - Join Clinical Trial NCTNCT03982394

How to Join This Clinical Trial - NCTNCT03982394

Learn how to participate in this clinical trial studying an investigational therapy for Chronic Plaque Psoriasis. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Chronic Plaque Psoriasis
Treatment Being Tested
Investigational treatment
Study Phase
Clinical trial phase - Research study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT03982394 - 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 302 locations. Find a study site near you:

Clinical Research Site

Lomas de Zamora, Buenos Aires 1832 - Argentina

Status: Contact for availability

Clinical Research Site

Pilar, Buenos Aires 1629 - Argentina

Status: Contact for availability

Clinical Research Site

Ciudad Autonoma Buenos Aires, Ciudad Autonoma De Buenos Aires 1114 - Argentina

Status: Contact for availability

Clinical Research Site

Ciudad Autonoma de Buenos Aire, Ciudad Autonoma De Buenos Aires 1023 - Argentina

Status: Contact for availability

Clinical Research Site

Ciudad Autonoma de Buenos Aire, Ciudad Autonoma De Buenos Aires 1055 - Argentina

Status: Contact for availability

Clinical Research Site

Ciudad Autonoma de Buenos Aire, Ciudad Autonoma De Buenos Aires 1425 - Argentina

Status: Contact for availability

Clinical Research Site

Ciudad Autonoma de Buenos Aire, Ciudad Autonoma De Buenos Aires 1425 - Argentina

Status: Contact for availability

Clinical Research Site

Ciudad Autonoma de Buenos Aire, Ciudad Autonoma De Buenos Aires 1425 - Argentina

Status: Contact for availability

Clinical Research Site

Buenos Aires, 1024 - Argentina

Status: Contact for availability

Clinical Research Site

Caba, C1199ABB - Argentina

Status: Contact for availability

And 292 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this clinical trial for Chronic Plaque Psoriasis:

  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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