Patient Guide: A Study in Participants With Major Depressive Disorder (MDD) With Anhedonia and Inadequate Response to Current Antidepressant Therapy Including a Selective Serotonin Reuptake Inhibitor (SSRI) or Serotonin Norepinephrine Reuptake Inhibitor (SNRI)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 94 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05841030
Status: ACTIVE_NOT_RECRUITING
Condition: Depressive Disorder, Major
Phase: Not Specified

Where You Can Participate

This study is available at 94 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Homewood, Alabama
  • • California City, California
  • • And 91 more locations

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A Study in Participants With Major Depressive Disorder (MDD) With Anhedonia and Inadequate Response to Current Antidepressant Therapy Including a Selective Serotonin Reuptake Inhibitor (SSRI) or Serotonin Norepinephrine Reuptake Inhibitor (SNRI) - Join Clinical Trial NCTNCT05841030

How to Join This Clinical Trial - NCTNCT05841030

Learn how to participate in this Not Specified trial studying an investigational therapy for Depressive Disorder, Major. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Depressive Disorder, Major
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05841030 - 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 94 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35233 - United States

Status: Contact for availability

Clinical Research Site

Homewood, Alabama 35209 - United States

Status: Contact for availability

Clinical Research Site

California City, California 92626 - United States

Status: Contact for availability

Clinical Research Site

Farmington, Connecticut 06030 - United States

Status: Contact for availability

Clinical Research Site

Saint Augustine, Florida 32086 - United States

Status: Contact for availability

Clinical Research Site

Sarasota, Florida 34237 - United States

Status: Contact for availability

Clinical Research Site

Tampa, Florida 33629 - United States

Status: Contact for availability

Clinical Research Site

Atlanta, Georgia 30338 - United States

Status: Contact for availability

Clinical Research Site

Marietta, Georgia 30060 - United States

Status: Contact for availability

Clinical Research Site

Chicago, Illinois 60637 - United States

Status: Contact for availability

And 84 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 Depressive Disorder, Major:

  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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