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Cyclic vs. Constant Estradiol: Regimens' Effects on Brain Health (CEREBRA)

16. September 2026 aktualisiert von: University of Colorado, Denver

Cyclic vs. Constant Estradiol: Regimens' Effects on Brain Health (CEREBRA Study)

The purpose of this study is to learn more about how estradiol patch treatment affects brain processes, health, and wellbeing.

Studienübersicht

Studientyp

Interventionell

Einschreibung (Geschätzt)

40

Phase

  • Phase 4

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studienorte

    • Colorado
      • Aurora, Colorado, Vereinigte Staaten, 80045
        • Rekrutierung
        • University of Colorado Anschutz
        • Kontakt:
        • Hauptermittler:
          • Neill Epperson, MD

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

38 Jahre bis 60 Jahre (Erwachsene)

Akzeptiert gesunde Freiwillige

Ja

Studienberechtigte Geschlechter

Weiblich

Beschreibung

Inclusion Criteria:

  1. Ages 38 to 60.
  2. Ability to give written informed consent.
  3. Fluent in written and verbal English, though may use Spanish to speak with study staff if preferred. This criterion is based on methodological necessity and feasibility, to ensure participants can accurately understand task instructions and questionnaire items which are available only in English for this pilot study.
  4. Participants must be up to date on age-appropriate cancer screening. Specifically, participants must have had a pap smear within the previous 3 years and a mammogram within the previous 2 years (American College of Obstetricians and Gynecologists, 2026; Health Resources and Services Administration, n.d.). Documentation may be requested to verify screening history.
  5. Have estradiol level below 40 pg/ml and follicle stimulating hormone (FSH) level above 25 at Van Visit Day 1. Individuals with high estradiol or low FSH levels may be retested, and eligibility determination will be at the discretion of the Principal Investigator (PI).
  6. Report final menstrual period (FMP) occurred between 12 months and 48 months at the time of screening.
  7. Right-handed.
  8. Participants are required to have at least some college education. Setting a minimum education level reduces variability due to educational disparities and supports the validity and interpretability of cognitive performance data. These tasks involve higher-order verbal learning, memory, and executive processes that can be strongly influenced by educational attainment. The investigators will re-evaluate this criterion in future larger-scale studies as resources allow.

Exclusion Criteria:

  1. Current psychiatric diagnosis as assessed by the Mini International Neuropsychiatric Interview (MINI, Sheehan et al., 1998).
  2. Active psychiatric illness within the previous 12 months or lifetime diagnosis of a psychotic disorder.
  3. Current use of antipsychotic medications or mood stabilizers. Participants may have sporadic use of benzodiazepines during the course of the study as long as they can forgo use at least 4 days prior to study procedures.
  4. Current or history of substance use disorder within previous 12 months. However, individuals with mild disorders, disorders solely limited to cannabis or alcohol, and/or those who have achieved close to one year of remission may be eligible at the discretion of the PI.
  5. Chronic use of steroid medication and other medications that could impact immune function and alter glucocorticoid levels.
  6. Inability to forgo use of non-steroidal anti-inflammatory medications for 4 days prior to the Baseline Visit, Van Visits, and Follow Up Visit.
  7. Any current or recent medical, psychiatric or social condition which, in the investigator's opinion, is likely to interfere with the conduct of the study, confound the interpretation of study results, or endanger the subject's well-being.
  8. Use of systemic hormone therapy (including but not limited to estradiol, progesterone, testosterone, combined hormonal contraceptives, and other systemic hormonal preparations) within 3 months prior to study enrollment. Use of local vaginal estrogen therapy (e.g., vaginal cream or Estring) is permitted. For participants with a history of systemic hormone use, the study investigator may review treatment history to determine whether postmenopausal status can be confirmed.
  9. History of suicidal behavior within the past 2 years
  10. Undiagnosed abnormal genital bleeding.
  11. Known, suspected, or history of breast cancer.
  12. Active deep vein thrombosis, pulmonary embolism, or history of these conditions.
  13. History of cardiovascular disease
  14. Known liver dysfunction or disease.
  15. Needle phobia or history of vasovagal response to phlebotomy.
  16. History of clinically relevant claustrophobia or inability to tolerate a scanning environment in the past.
  17. Metal in body unsafe for magnetic resonance imaging (MRI) or other conditions that would make MRI unsafe for participants (i.e., aneurysm clip, cardiac pacemaker, etc.).
  18. Current treatment with Central nervous system (CNS) depressants (e.g., opioids, benzodiazepines).
  19. Treatment with corticosteroids within the past 30 days.
  20. Known allergy to progesterone or peanut allergy.
  21. Any history of chemotherapy as negative effects on cognitive performance have been reported for years post cessation of treatment (Guida et al., 2021; Koppelmans et al., 2012).

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Unterstützende Pflege
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Cyclic Estradiol

Transdermal estradiol 100 mcg/day patch applied for 5 days every 21 days for approximately 12 weeks.

Participants randomized to the cyclic estradiol group apply a transdermal estradiol patch delivering 100 mcg/day for 5 days every 21 days over approximately 12 weeks. The patch is removed on the fifth day of each treatment cycle. The final patch is worn for 7 days.

Andere Namen:
  • Estradiol Patch
  • Transdermal Estradiol
Experimental: Continuous Estradiol

Transdermal estradiol 100 mcg/day patch worn continuously and replaced every 6 days for approximately 12 weeks.

Participants randomized to the continuous estradiol group apply a transdermal estradiol patch delivering 100 mcg/day continuously for approximately 12 weeks. The patch is replaced every 6 days and worn throughout the treatment period. The final patch is worn for 7 days.

Andere Namen:
  • Estradiol Patch
  • Transdermal Estradiol

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change in Dorsolateral Prefrontal Cortex (dlPFC) activation during working memory task in women receiving either cyclic or continuous estradiol administration.
Zeitfenster: Baseline and approximately 12 weeks after initiation of study treatment

Description: Dorsolateral prefrontal cortex (dlPFC) activation will be measured during performance of the letter N-back task using functional magnetic resonance imaging (fMRI). Change scores will be calculated from baseline to follow-up.

Baseline and approximately 12 weeks after initiation of study treatment
Change from baseline in extracellular vesicle concentration.
Zeitfenster: Baseline, Days 1-4, Days 21-24, and approximately 12 weeks after treatment initiation

Extracellular vesicle (EV) concentration will be measured from plasma samples and reported as particles per milliliter (particles/mL). Changes from baseline will be assessed following cyclic or continuous estradiol administration.

Baseline, Days 1-4, Days 21-24, and approximately 12 weeks after treatment initiation
Change from baseline in extracellular vesicle size.
Zeitfenster: Baseline, Days 1-4, Days 21-24, and approximately 12 weeks after treatment initiation

Extracellular vesicle (EV) size will be measured from plasma samples and reported in nanometers (nm). Changes from baseline will be assessed following cyclic or continuous estradiol administration.

Baseline, Days 1-4, Days 21-24, and approximately 12 weeks after treatment initiation
Change from baseline in extracellular vesicle zeta potential.
Zeitfenster: Baseline, Days 1-4, Days 21-24, and approximately 12 weeks after treatment initiation

Extracellular vesicle (EV) zeta potential will be measured from plasma samples and reported in millivolts (mV). Changes from baseline will be assessed following cyclic or continuous estradiol administration.

Baseline, Days 1-4, Days 21-24, and approximately 12 weeks after treatment initiation
Change in C-reactive protein concentration.
Zeitfenster: Baseline and approximately 12 weeks after initiation of study treatment

Serum C-reactive protein concentration measured using the Meso Scale Discovery (MSD) V-PLEX Neuroinflammation Panel.

Baseline and approximately 12 weeks after initiation of study treatment
Change in interleukin concentration.
Zeitfenster: Baseline and approximately 12 weeks after initiation of study treatment

Interleukin concentration measured using the MSD V-Plex Neuroinflammation Panel.

Baseline and approximately 12 weeks after initiation of study treatment
Change in cytokine concentration.
Zeitfenster: Baseline and approximately 12 weeks after initiation of study treatment

Cytokine concentration measured using the MSD V-Plex Neuroinflammation Panel.

Baseline and approximately 12 weeks after initiation of study treatment
Change in chemokine concentration.
Zeitfenster: Baseline and approximately 12 weeks after initiation of study treatment

Chemokine concentration measured using the MSD V-Plex Neuroinflammation Panel.

Baseline and approximately 12 weeks after initiation of study treatment
Change in growth factor concentration.
Zeitfenster: Baseline and approximately 12 weeks after initiation of study treatment

Growth factor concentration measured using the MSD V-Plex Neuroinflammation Panel.

Baseline and approximately 12 weeks after initiation of study treatment

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change in executive function symptoms on the Brown Attention-Deficit Disorder Scale (BADDS).
Zeitfenster: Baseline and approximately 12 weeks after initiation of study treatment

The BADDS is a validated 40-item self-report measure of executive function difficulties. Total scores range from 0 to 120, with higher scores indicating greater executive dysfunction.

Baseline and approximately 12 weeks after initiation of study treatment
Change in perceived stress on the Perceived Stress Scale (PSS).
Zeitfenster: Baseline and approximately 12 weeks after initiation of study treatment

The PSS is a 10-item self-report measure of perceived stress. Total scores range from 0 to 40, with higher scores indicating greater perceived stress.

Baseline and approximately 12 weeks after initiation of study treatment
Change in depressive symptoms on the Center for Epidemiologic Studies Depression Scale (CES-D).
Zeitfenster: Baseline and approximately 12 weeks after initiation of study treatment

The CES-D is a 20-item self-report measure of depressive symptoms. Total scores range from 0 to 60, with higher scores indicating greater severity of depressive symptoms.

Baseline and approximately 12 weeks after initiation of study treatment
Change in anxiety symptoms on the Generalized Anxiety Disorder-7 (GAD-7).
Zeitfenster: Baseline and approximately 12 weeks after initiation of study treatment

The GAD-7 is a 7-item self-report measure of anxiety symptoms. Total scores range from 0 to 21, with higher scores indicating greater anxiety symptom severity.

Baseline and approximately 12 weeks after initiation of study treatment
Change in hair cortisol concentration.
Zeitfenster: Baseline and approximately 12 weeks after initiation of study treatment

Hair cortisol concentration is a biomarker of chronic hypothalamic-pituitary-adrenal axis activity. Higher concentrations indicate greater cumulative cortisol exposure over the preceding approximately three months.

Baseline and approximately 12 weeks after initiation of study treatment

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Mitarbeiter

Ermittler

  • Hauptermittler: Neill Epperson, MD, University of Colorado, Denver

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

15. Juli 2026

Primärer Abschluss (Geschätzt)

15. Juli 2028

Studienabschluss (Geschätzt)

15. Juli 2028

Studienanmeldedaten

Zuerst eingereicht

28. August 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

16. September 2026

Zuerst gepostet (Tatsächlich)

21. September 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

21. September 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

16. September 2026

Zuletzt verifiziert

1. September 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Ja

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Produkt, das in den USA hergestellt und aus den USA exportiert wird

Nein

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