Patient Guide: Effect of Naltrexone Hydrochloride ER and Bupropion Hydrochloride ER Combination (Contrave®/Mysimba®) on Major Adverse Cardiovascular Events (MACE)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 134 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06098079
Status: 🟢 Enrolling Now
Condition: Obesity
Phase: PHASE4

Where You Can Participate

This study is available at 134 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Cullman, Alabama
  • • Mobile, Alabama
  • • And 131 more locations

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Effect of Naltrexone Hydrochloride ER and Bupropion Hydrochloride ER Combination (Contrave®/Mysimba®) on Major Adverse Cardiovascular Events (MACE) - Join Clinical Trial NCTNCT06098079

How to Join This Clinical Trial - NCTNCT06098079

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

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Obesity
Treatment Being Tested
Investigational treatment
Study Phase
PHASE4 - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06098079 - 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 134 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35216 - United States

Status: RECRUITING

Clinical Research Site

Cullman, Alabama 35055 - United States

Status: TERMINATED

Clinical Research Site

Mobile, Alabama 36608 - United States

Status: RECRUITING

Clinical Research Site

Mobile, Alabama 36608 - United States

Status: RECRUITING

Clinical Research Site

Glendale, Arizona 85304 - United States

Status: RECRUITING

Clinical Research Site

Glendale, Arizona 85306 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Mesa, Arizona 85213 - United States

Status: RECRUITING

Clinical Research Site

Phoenix, Arizona 85006 - United States

Status: RECRUITING

Clinical Research Site

Tempe, Arizona 85283 - United States

Status: RECRUITING

Clinical Research Site

Anderson, California 90247 - United States

Status: RECRUITING

And 124 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

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

  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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