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CompletedNCT05537675177LumenUpdated Nov 30, 2023

Semi-automated Segmentation Methods of SSTR PET for Dosimetry Prediction

An observational study in Refractory Meningioma, sponsored by Central Hospital, Nancy, France. Completed at 1 site in France. Open to participants aged 18 Years to 90 Years. Per ClinicalTrials.gov, last updated 2023-11-30.

Sponsored by Central Hospital, Nancy, France · Observational

Study type
Observational
Model
Other
Time perspective
Retrospective
Enrollment
20
Ages
18 Years to 90 Years
Sex
All
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Study summary

Tumor dosimetry with somatostatin receptor-targeted peptide receptor radionuclide therapy (SSTR-targeted PRRT) by 177Lutetium-DOTATATE might contribute to improve follow-up and treatment response of refractory meningiomas. This study aims to evaluate Standard Uptake Value mean (SUVmean) as a tumoral absorbed dose predictive predictive factor and propose semi-automated segmentation method to determine metabolic tumor volume with pretherapeutic 68-Gallium-DOTATOC PET.

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Conditions studied

  • Refractory Meningioma

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In context

Meningioma

226 studies on the registry are indexed under Meningioma; 87 are open to participants now.

This study's enrollment of 20 is below the median of 132 across 56 observational studies indexed under Meningioma.

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Lead sponsor

Central Hospital, Nancy, France is the lead sponsor of 778 studies on the registry; 183 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

20 patients with meningioma will be included in this study, and 10 patients of 20 will have been treated with Lutathera®.

Inclusion criteria

  • Patients with meningioma

Exclusion criteria

Exclusion Criteria:

  • PET scan not available
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Study design

Observational model
Other
Time perspective
Retrospective
Enrollment
20 participants (actual)
Patient registry
No

Groups and cohorts

  • 20 patients with meningioma

    20 meningioma patients will be included in this study, 10 of whom will have been treated with Lutathera®.

    Other: To evaluate the SUVmean (Standard Uptake Value) as a predictive factor of the tumor absorbed dose compared to the SUVmax

  • 10 patients will have been treated with Lutathera®.

    10 patients of the 20 will have been treated with Lutathera®.

    Other: To evaluate the SUVmean (Standard Uptake Value) as a predictive factor of the tumor absorbed dose compared to the SUVmax

Interventions

  • OtherTo evaluate the SUVmean (Standard Uptake Value) as a predictive factor of the tumor absorbed dose compared to the SUVmax

    Measure SUVmean (Standard Uptake Value) and SUVmax on PET exams

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What researchers measure

Primary outcomes

  1. To evaluate the SUVmean (Standard Uptake Value)as a predictive factor of the tumor absorbed dose compared to the SUVmax

    Measurements of SUVmean and SUVmax at the lesion level on 68Ga-DOTATOC PET/CT Correlation between SUVmean and max measurements with tumor absorbed doses.

    Time frame: 2 months

  2. To propose a semi-automated segmentation

    Propose a semi-automated segmentation method for determining metabolic tumor volume with pretherapy DOTATOC labelled with gallium-68 PET. (68Ga-DOTATOC PET)

    Time frame: 1 month

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Study locations

1 site
  • Nuclear medicine Department CHRU de NANCY
    Vandoeuvre les Nancy cedex, 54511, France
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 30, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05537675
Lead sponsor
Central Hospital, Nancy, France
Responsible party
Antoine VERGER (Principal investigator, Central Hospital, Nancy, France) — Principal investigator
First posted
Sep 13, 2022
Start date
Oct 1, 2022
Primary completion
Nov 6, 2022
Completion
Nov 30, 2022
Last update
Nov 30, 2023

Study contacts

Anne-Sophie HUE, MSc
study director · CHRU Nancy

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2023. You cannot join it, but the record below documents what was studied.

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