Tumor Absorbed Dose-Response Relationship in Patients Treated With 177Lu-DOTATATE for Meningioma
DATUM
1 other identifier
observational
11
1 country
2
Brief Summary
The hypothesis for this study is that there is a dose-response relationship in patients treated with 177Lu-DOTATATE for meningiomas.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Nov 2024
Shorter than P25 for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 6, 2024
CompletedFirst Posted
Study publicly available on registry
September 26, 2024
CompletedStudy Start
First participant enrolled
November 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
February 25, 2025
CompletedMarch 4, 2025
February 1, 2025
2 months
June 6, 2024
February 28, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Diagnostic accuracy for progression free survival
Accuracy of tumor dosimetry to predict 6-month progression-free survival.
Day 1
Secondary Outcomes (1)
Diagnostic accuracy for overal survival
Day 1
Study Arms (1)
Patients treated with 177Lu-DOTATATE for meningioma
Patients treated with 177Lu-DOTATATE for meningioma at the Nancy's hospital who met the treatment criteria of the Compassionate Prescribing Framework and received a scintigraphy at D1, D4 and D7 (± 1 day)
Interventions
The tumoral dosimetry has been done on patient after treatment by 177Lu-DOTATATE Theses patients performed a scintigraphy exam at D1, D4 and D7 after the treatment
Eligibility Criteria
patients treated with 177Lu-DOTATATE for meningioma at Nancy University Hospital
You may qualify if:
- patients treated for menigioma at nancy hospital
- patients who performed 3 scintigraphics exams during there treatment
You may not qualify if:
- patients deprived of liberty
- patient who refused to collect data retrospectively
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
CHRU de NANCY
Vandœuvre-lès-Nancy, 54511, France
Nuclear medicine Department CHRU de NANCY
Vandœuvre-lès-Nancy, 54511, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
June 6, 2024
First Posted
September 26, 2024
Study Start
November 1, 2024
Primary Completion
January 1, 2025
Study Completion
February 25, 2025
Last Updated
March 4, 2025
Record last verified: 2025-02
Data Sharing
- IPD Sharing
- Will not share