Pseudomyxoma Peritonei Clinical Trials

Find Pseudomyxoma Peritonei Clinical Trials Near You

The ACPMP Research Foundation Appendix Cancer/PMP Patient Registry

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

ACPMP's first-ever patient-powered global patient registry/natural history study collects patient and caregiver information and data to fuel clinical trials and drive breakthroughs for appendix cancer and PMP. We've invested the time and resources to make our Registry regulatory grade. Our Registry operates under active, ongoing Institutional Review Board (IRB) oversight by independent ethicists. It is powered by NORD's IAMRARE®, an industry gold standard platform built to be consistent with FDA's best thinking on natural history studies.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Diagnosis of appendix cancer.

• Meets the study inclusion criteria for participation.

• Participant or, when applicable, a legally authorized representative (LAR) is able to provide informed consent and enter information into the Registry.

• A designated representative may provide retrospective information for an individual who died from appendix cancer, as permitted by the study protocol.

Locations
United States
Pennsylvania
ACPMP
RECRUITING
Springfield
Contact Information
Primary
Margaret Najarian
patientregistry@acpmp.org
(833) 227-6773
Time Frame
Start Date: 2026-02-02
Estimated Completion Date: 2030-02-01
Participants
Target number of participants: 10000
Treatments
Participants with Appendix Cancer and/or Pseudomyxoma Peritonei (PMP)
Individuals diagnosed with appendix cancer and/or Pseudomyxoma Peritonei (PMP) who enroll in the ACPMP Research Foundation Appendix Cancer/PMP Patient Registry. Participants, caregivers, or authorized representatives provide health and disease-related information through online surveys and may periodically update their information over time.
Related Therapeutic Areas
Sponsors
Leads: Appendix Cancer Pseudomyxoma Peritonei Research Foundation
Collaborators: National Organization for Rare Disorders

This content was sourced from clinicaltrials.gov