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Phase 3 N=64 Randomized Double-blind Treatment

Estrogen and Fear in PTSD

PTSD

Enrolled (actual)
64
Serious AEs
0.0%
Results posted
Jan 2026
Primary outcome: Primary: Change in Amygdala Activation as Measured by Functional Magnetic Resonance Imaging (fMRI) Blood Oxygen Level Dependent (BOLD) Signal — 0.534; -0.0037 beta weights

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Estradiol (Drug); Placebo oral tablet (Drug); Prolonged Exposure (PE) therapy (Behavioral)
Age
Adult · 18+ yrs
Sex
Female
Sponsor
The University of Texas Health Science Center, Houston
Primary completion
May 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Amygdala Activation as Measured by Functional Magnetic Resonance Imaging (fMRI) Blood Oxygen Level Dependent (BOLD) Signal
0.534; -0.0037
PRIMARY
Change in Dorsal Anterior Cingulate Cortex (dACC) Activation as Measured by Functional Magnetic Resonance Imaging (fMRI) Blood Oxygen Level Dependent (BOLD) Signal
0.292; -0.0276
PRIMARY
Change in Ventromedial Prefrontal Cortex (vmPFC) Activation as Measured by Functional Magnetic Resonance Imaging (fMRI) Blood Oxygen Level Dependent (BOLD) Signal
0.512; -0.118
PRIMARY
Change in Hippocampus Activation as Measured by Functional Magnetic Resonance Imaging (fMRI) Blood Oxygen Level Dependent (BOLD) Signal
0.341; -0.0606
SECONDARY
Skin Conductance Response (SCR) During Recall
0.000479; 0.0894
SECONDARY
Skin Conductance Response (SCR) During Recall
0.000479; 0.0894
SECONDARY
Change in PTSD Symptom Assessed by the Clinician-Administered PTSD Scale for DSM-5 (CAPS)
-22.83; -23.62
SECONDARY
Change in PTSD Symptom Assessed by the Clinician-Administered PTSD Scale for DSM-5 (CAPS)
-22.83; -23.62
SECONDARY
Change in PTSD Symptom Assessed by the Clinician-Administered PTSD Scale for DSM-5 (CAPS)
-22.83; -23.62

Summary

The purpose of this research study is to determine if taking a pill of estradiol (E2) together with prolonged exposure (PE) therapy can improve this treatment outcome in women diagnosed with Post-Traumatic Stress Disorder (PTSD). 80 subjects will take part in this research study across UTHealth Houston and UPenn (40 subjects at each site). Participants will be randomized into one of two groups, PE + E2 or PE + placebo. The study will include preliminary screening and baseline visits, experimental visits, and therapy visits over the course of six weeks. Several follow-up visits will take place.

Eligibility Criteria

Inclusion Criteria

  • Female, 18-45 years of age
  • Chronic (at least one month post-trauma) DSM-5 FULL PTSD diagnosis OR subPTSD diagnosis (subPTSD defined as: meeting criterion A, F, G, H, and clusters B, C, and at least 1 of the clusters D or E.)
  • CAPS-5 Past Month score ≥ 20
  • Criterion A traumatic event
  • Stable medications for 3 or more months by the time of study entrance (with the exception of benzodiazepines)
  • Women on oral contraceptives, specifically those using monophasic or biphasic of first, second, third or fourth generation with up to 35mcg of ethinyl estradiol; OR using etonogestrel / ethinyl estradiol 0.120mg/0.015mg per day vaginal ring birth control; OR using the norelgestromin / ethinyl estradiol 0.150mg/0.035mg per day transdermal patch birth control.
  • Willing and able to provide informed consent

Exclusion Criteria

  • Diagnosis of bipolar I disorder with a past year manic episode
  • Diagnosis of a psychotic disorder or psychotic symptoms that would interfere with the ability to focus on posttraumatic stress disorder (PTSD) in clinic, as determined by clinical judgment.
  • Diagnosis of moderate or severe substance use disorder that would interfere with the ability to focus on posttraumatic stress disorder (PTSD) in clinic, as determined by clinical judgment.
  • Cognitive impairment that would interfere with the ability to focus on posttraumatic stress disorder (PTSD) in clinic, as determined by clinical judgment.
  • History of neurological disease (that involves the brain), seizure, or significant head trauma (i.e., extended loss of consciousness, neurological sequelae, or known structural brain lesion).
  • Suicidal ideation with imminent risk that warrants a higher level of care.
  • Concurrent trauma focused psychotherapy
  • Pregnancy (to be ruled out by urine ß-HCG).
  • Metallic implants or devices contraindicating magnetic resonance imaging by interfering with patient safety or fMRI data collection. Cases will be cleared by the Principal Investigator and/or Baylor College of Medicine (Imaging).
  • History of breast cancer or hormone-responsive cancer.
  • Use of benzodiazepines
  • Self-injurious behavior that involves suicidal intent, requires medical attention, or occurs daily.
  • High risk of adverse emotional or behavioral reaction, and/or an inability to understand study procedures or the informed consent process, based on investigator/clinician clinical evaluation (e.g., evidence of serious personality disorder, antisocial behavior, serious current stressors, lack of meaningful social support)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04192266). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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