Patient Guide: Optilume PoST AppRoval Clinical Evaluation of Andrology ParaMeters

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 9 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05383274
Status: 🟢 Enrolling Now
Condition: Urethral Stricture
Phase: PHASE4

Where You Can Participate

This study is available at 9 locations across the country.

Top locations include:
  • • Little Rock, Arkansas
  • • Orlando, Florida
  • • Tampa, Florida
  • • And 6 more locations

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Optilume PoST AppRoval Clinical Evaluation of Andrology ParaMeters - Join Clinical Trial NCTNCT05383274

How to Join This Clinical Trial - NCTNCT05383274

Learn how to participate in this PHASE4 trial studying an investigational therapy for Urethral Stricture. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Urethral Stricture
Treatment Being Tested
Investigational treatment
Study Phase
PHASE4 - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05383274 - 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 9 locations. Find a study site near you:

Clinical Research Site

Little Rock, Arkansas 72211 - United States

Status: RECRUITING

Clinical Research Site

Orlando, Florida 32806 - United States

Status: RECRUITING

Clinical Research Site

Tampa, Florida 33615 - United States

Status: RECRUITING

Clinical Research Site

Shreveport, Louisiana 71106 - United States

Status: COMPLETED

Clinical Research Site

Hanover, Maryland 21076 - United States

Status: COMPLETED

Clinical Research Site

Las Vegas, Nevada 89144 - United States

Status: RECRUITING

Clinical Research Site

Millburn, New Jersey 07041 - United States

Status: COMPLETED

Clinical Research Site

Cheektowaga, New York 14225 - United States

Status: RECRUITING

Clinical Research Site

Dallas, Texas 75231 - United States

Status: RECRUITING

How to Enroll in This Study

To learn more about participating in this PHASE4 clinical trial for Urethral Stricture:

  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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