Patient Guide: Long Term Observational Study to Collect in a Real-world populatIon Data on the Treatment Pattern of secukinumAb in Adult Patients With Moderate to Severe Hidradenitis Suppurativa.

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 80 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05921994
Status: ACTIVE_NOT_RECRUITING
Condition: Hidradenitis Suppurativa
Phase: Not Specified

Where You Can Participate

This study is available at 80 locations across the country.

Top locations include:
  • • Freiburg im Breisgau, Baden-Wurttemberg
  • • Kulmbach, Bavaria
  • • Lauf an der Pegnitz, Bavaria
  • • And 77 more locations

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Long Term Observational Study to Collect in a Real-world populatIon Data on the Treatment Pattern of secukinumAb in Adult Patients With Moderate to Severe Hidradenitis Suppurativa. - Join Clinical Trial NCTNCT05921994

How to Join This Clinical Trial - NCTNCT05921994

Learn how to participate in this Not Specified trial studying an investigational therapy for Hidradenitis Suppurativa. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Hidradenitis Suppurativa
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05921994 - 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 80 locations. Find a study site near you:

Clinical Research Site

Freiburg im Breisgau, Baden-Wurttemberg 79068 - Germany

Status: Contact for availability

Clinical Research Site

Kulmbach, Bavaria 95326 - Germany

Status: Contact for availability

Clinical Research Site

Lauf an der Pegnitz, Bavaria 91207 - Germany

Status: Contact for availability

Clinical Research Site

Hamburg, City state of Hamburg 22549 - Germany

Status: Contact for availability

Clinical Research Site

Lingen Ems, Lower Saxony 49809 - Germany

Status: Contact for availability

Clinical Research Site

Kröpelin, Mecklenburg-Vorpommern 18236 - Germany

Status: Contact for availability

Clinical Research Site

Krefeld, North Rhine-Westphalia 47798 - Germany

Status: Contact for availability

Clinical Research Site

Mainz, Rhineland-Palatinate 55128 - Germany

Status: Contact for availability

Clinical Research Site

Dresden, Saxony 01307 - Germany

Status: Contact for availability

Clinical Research Site

Leipzig, Saxony 04207 - Germany

Status: Contact for availability

And 70 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Hidradenitis Suppurativa:

  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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