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Trial · NCT04711135

Results by group28

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Absorbed Radiation Doses in Target OrganGEP-NETKidney0.71Standard Deviation 0.25Gy/GBq
Absorbed Radiation Doses in Target OrganPPGLKidney0.82Standard Deviation 0.32Gy/GBq
Absorbed Radiation Doses in Target OrganGEP-NETPituitary1.2Standard Deviation 0.43Gy/GBq
Absorbed Radiation Doses in Target OrganPPGLPituitary1.0Standard Deviation 0.45Gy/GBq
Absorbed Radiation Doses in Target OrganGEP-NETRed Marrow (Blood)0.024Standard Deviation 0.0035Gy/GBq
Absorbed Radiation Doses in Target OrganPPGLRed Marrow (Blood)0.028Standard Deviation 0.0052Gy/GBq
Absorbed Radiation Doses in Target OrganGEP-NETRed Marrow (Image)0.043Standard Deviation 0.018Gy/GBq
Absorbed Radiation Doses in Target OrganPPGLRed Marrow (Image)0.067Standard Deviation 0.028Gy/GBq
Absorbed Radiation Doses in Target OrganGEP-NETSpleen0.63Standard Deviation 0.39Gy/GBq
Absorbed Radiation Doses in Target OrganPPGLSpleen0.82Standard Deviation 0.17Gy/GBq
Absorbed Radiation Doses in Target OrganGEP-NETUrinary Bladder Wall0.50Standard Deviation 0.034Gy/GBq
Absorbed Radiation Doses in Target OrganPPGLUrinary Bladder Wall0.59Standard Deviation 0.096Gy/GBq
Absorbed Radiation Doses in Target OrganGEP-NETTotal Body0.040Standard Deviation 0.013Gy/GBq
Absorbed Radiation Doses in Target OrganPPGLTotal Body0.041Standard Deviation 0.0073Gy/GBq
Incidence of Adverse Events (AEs) and Lab Toxicities After 1st Lutathera AdministrationGEP-NET4Participants
Incidence of Adverse Events (AEs) and Lab Toxicities After 1st Lutathera AdministrationPPGL6Participants
Incidence of Adverse Events (AEs) During Treatment and Short-term Follow-upGEP-NETAEs during Lutathera treatment4Participants
Incidence of Adverse Events (AEs) During Treatment and Short-term Follow-upPPGLAEs during Lutathera treatment7Participants
Incidence of Adverse Events (AEs) During Treatment and Short-term Follow-upGEP-NETAEs during short-term follow-up1Participants
Incidence of Adverse Events (AEs) During Treatment and Short-term Follow-upPPGLAEs during short-term follow-up3Participants

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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