Under construction – not a live service
Sign in

NCT04770831Withdrawn

Patients Who Receive 131 I-MIBG

An Observational Study of Patients With Recurrent Progressive or Refractory Neuroblastoma or Malignant Pheochromocytoma or Paraganglioma Who Receive 131 I- MIBG

Source: ClinicalTrials.gov · Last updated 14 Dec 2022

Reason given: difficult enrollment, no subjects consented or enrolled

Brief summary (registry, in English)

This study is for patients who have have neuroblastoma, pheochromocytoma, or paraganglioma that has come back (relapsed) after treatment or has not gotten better (refractory) with standard treatment. The purpose of this study is to evaluate quality of life and response rate to 131 I-MIBG treatment.

Status (registry)
Withdrawn
Study type
Observational
Enrollment
0 (actual)
First submitted
16 Feb 2021
Start date
10 Mar 2021
Primary completion date
Dec 2024
Lead sponsor
Wake Forest University Health Sciences
NCT number
NCT04770831

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior enrollment on LCI-PED-NEU-MIBG-001 trial.

Other

  • Subjects meeting the criteria below may not participate in the study:

Who the study is looking for

  • Subject must meet all of the following applicable inclusion criteria to participate in this study:
  • Written informed consent, and assent where applicable, and HIPAA authorization for release of personal health information. NOTE: HIPAA authorization may be included in the informed consent or obtained separately.
  • Age greater than or equal to 1 years and less than or equal to 30 years at the time of therapy.
  • Subject is scheduled to receive 131 I-MIBG therapy.
  • Diagnosis of refractory, progressive or relapsed Neuroblastoma, Malignant Paraganglioma, Malignant Pheochromocytoma or other Neuroendocrine Tumors.
  • As determined by the enrolling physician, ability of the subject and parent/caregiver to understand and comply with study procedures for the entire length of the study.

Age in the registry: 1 year to 30 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Levine Cancer InstituteCharlotteUnited StatesUnknown status

Are you the coordinator? Confirm the details

This page is information, not medical advice. Discuss any trial with your doctor.