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Trial · NCT07509840

Registered outcomes12

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryEgg retrieval in response to controlled ovarian hyperstimulation4 to 6 months after rituximab/placebo treatment.Egg retrieval (yes/no) in response to controlled ovarian hyperstimulation at 4 to 6 months after rituximab treatment compared to placebo.
SecondaryOccurrence of spontaneous menstrual bleeding19-month study period from baseline to end of study.Occurrence of spontaneous menstrual bleeding (yes/no) at any point during the 19-month study period.
SecondaryProportion of participants who achieve ovulationDuring 19 months from baseline to end of study.Proportion of participants who achieve ovulation (defined as serum progesterone \>10 nmol/L) at any time during the study period.
SecondaryChanges in serum follicle-stimulating hormoneFrom baseline to the end of the study period (19 months).Changes in serum follicle-stimulating hormone (FSH) IE/L levels from baseline to the end of the study period.
SecondaryChange in serum anti-Mullerian hormoneFrom baseline to the end of the study period (19 months).Changes in serum anti-Mullerian hormone (AMH) microgram/L levels from baseline to the end of the study period.
SecondaryChanges in B-cell countFrom baseline to the end of the study period (19 month).Changes in B-cell count x109/L from baseline to end of study.
SecondaryChanges in autoantibody indicesFrom baseline to the end of the study period (19 months)Changes in autoantibody indices from baseline to the end of the study period.
SecondaryChanges in immunoglobulin (IgG) levelsFrom baseline to the end of the study period (19 months).Changes in immunoglobulin (IgG) g/L levels from baseline to the end of the study period.
SecondaryChanges in quality of life scores, as measured by the Addison's Disease Quality of Life questionnaireFrom baseline to the end of the study period (19 months).Changes in quality of life scores, as measured by the validated instrument Addison's Disease Quality of Life (AddiQol) from baseline to the end of the study period.
SecondaryChanges in quality life scores, as measured by the Psychological General Well-being questionnaireFrom baseline to the end of the study period (19 months).Changes in quality life scores, as measured by the validated Psychological General Well-being (PGWB) from baseline to the end of the study period.
SecondaryChanges in quality of life scores, as measured by the Short Form Health SurveyFrom baseline to the end of the study period (19 months).Changes in quality of life scores as measured by the validated instrument Short Form Health Survey (SF-36) from baseline to the end of the study period.
SecondaryChanges in quality of life scores as measured by the Menopause Rating ScaleFrom baseline to the end of the study period (19 months).Changes in qualit of life scores, as measured by the validated Menopause Rating Scale (MRS) from baseline to the end of the study period.

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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GET https://conductscience.org/api/trials/v1/NCT07509840/registered