Patient Guide: Impact of a Multidisciplinary Assessment in Day Hospitalization Versus Standard Care on the Deployment of Supportive Oncology Care Recommended by the Personalized Post-cancer Plan in Patients at the End of Initial Treatment for Gynecological Ovarian and Endometrial Cancer Endometrial Cancer

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 13 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06553612
Status: 🟢 Enrolling Now
Condition: Gynecologic Cancer, Remission
Phase: NA

Where You Can Participate

This study is available at 13 locations across the country.

Top locations include:
  • • Besançon,
  • • Caen,
  • • Clermont-Ferrand,
  • • And 10 more locations

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Impact of a Multidisciplinary Assessment in Day Hospitalization Versus Standard Care on the Deployment of Supportive Oncology Care Recommended by the Personalized Post-cancer Plan in Patients at the End of Initial Treatment for Gynecological Ovarian and Endometrial Cancer Endometrial Cancer - Join Clinical Trial NCTNCT06553612

How to Join This Clinical Trial - NCTNCT06553612

Learn how to participate in this NA trial studying an investigational therapy for Gynecologic Cancer, Remission. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Gynecologic Cancer, Remission
Treatment Being Tested
Investigational treatment
Study Phase
NA - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06553612 - 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 13 locations. Find a study site near you:

Clinical Research Site

Besançon, - France

Status: RECRUITING

Clinical Research Site

Caen, - France

Status: RECRUITING

Clinical Research Site

Clermont-Ferrand, - France

Status: NOT_YET_RECRUITING

Clinical Research Site

Lyon, - France

Status: RECRUITING

Clinical Research Site

Paris, - France

Status: RECRUITING

Clinical Research Site

Paris, - France

Status: NOT_YET_RECRUITING

Clinical Research Site

Paris, - France

Status: NOT_YET_RECRUITING

Clinical Research Site

Paris, - France

Status: NOT_YET_RECRUITING

Clinical Research Site

Plérin, - France

Status: NOT_YET_RECRUITING

Clinical Research Site

Saint-Cloud, - France

Status: RECRUITING

And 3 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this NA clinical trial for Gynecologic Cancer, Remission:

  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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