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Phase 2 N=88 Randomized Triple-blind Treatment

Pregnenolone for Cognitive and Negative Symptoms in Schizophrenia

Schizophrenia · Schizoaffective Disorder

Enrolled (actual)
88
Serious AEs
8.0%
Results posted
Feb 2017
Primary outcome: Primary: MATRICS Consensus Cognitive Battery (MCCB) — 30.92; 30.32; 33.43; 32.76 T score

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Dietary Supplement: Pregnenolone (Drug); Placebo (Dietary_supplement)
Age
Adult, Older Adult · 21+ yrs
Sex
All
Sponsor
VA Office of Research and Development
Primary completion
Mar 2015

Outcome Measures

OutcomeResultp-value
PRIMARY
MATRICS Consensus Cognitive Battery (MCCB)
30.92; 30.32; 33.43; 32.76; 36.97; 34.25
PRIMARY
University of California Performance-based Skills Assessment (UPSA)
77.49; 76.68; 77.29; 80.12; 85.63; 82.03
PRIMARY
Brief Assessment of Cognition in Schizophrenia (BACS)
-1.37; -1.53; -1.11; -1.17; -0.79; -1.09
PRIMARY
Scale for the Assessment of Negative Symptoms(SANS)
26.92; 25.88; 23.87; 21.74; 21.00; 20.77
SECONDARY
The Calgary Depression Scale for Schizophrenia (CDSS)
2.84; 3.18; 2.39; 2.79; 2.68; 2.46
SECONDARY
Positive and Negative Syndrome Scale (PANSS)
65.74; 63.68; 61.47; 56.79; 59.10; 57.12
SECONDARY
Clinical Global Impressions (CGI) Scale
3.56; 3.58; 3.39; 3.39; 3.42; 3.24

Summary

This study will investigate adjunctive pregnenolone for patients with schizophrenia and schizoaffective disorder.

Eligibility Criteria

Inclusion Criteria

  • Diagnosis: DSM-IV/DSM-IV TR schizophrenia or schizoaffective disorder;
  • Gender: Males and Females;
  • Age: 21-65;
  • Caucasian or Non Caucasian;
  • Capable of providing informed consent;
  • Duration of illness equal to or greater than one year;
  • No change in antipsychotic medication in the previous eight weeks, no change in antipsychotic dose in the previous four weeks;
  • No benzodiazepine use in the past twelve hours prior to cognitive testing;
  • The patient cohort will be enriched for cognitive symptoms (Composite BACS scores = 0-3 standard deviations below the mean, assessed at the screening visit).

Exclusion Criteria

  • Subjects with a DSM-IV/DSM-IV TR diagnosis of alcohol or substance dependence (other than nicotine) within the last month;
  • Subjects with a history of significant head injury/trauma, as defined by one or more of the following:
  • Loss of consciousness (LOC) for more than 1 hour,
  • Recurring seizures resulting from the head injury,
  • Clear cognitive sequelae of the injury,
  • Cognitive rehabilitation following the injury;
  • Subjects with unstable medical illness or neurological illness (seizures, CVA);
  • Patients with hormone-sensitive tumors (such as breast, uterine, or prostate cancer);
  • Clinically significant abnormalities in physical examination , ECG, or laboratory assessments;
  • Pregnant women or women of child-bearing potential, who are either not surgically-sterile or not using appropriate methods of birth control (serum beta-human chorionic gonadotropin [HCG] will be performed at baseline, 4 weeks, and 8 weeks to exclude pregnancy);
  • Women who are breast-feeding;
  • Electroconvulsive therapy (ECT) treatment within the last 3 months;
  • Use of oral contraceptives or other hormonal supplementation such as estrogen. Although early studies suggested no effects on menstrual cycle, alterations in downstream metabolites of pregnenolone (such as estradiol) could theoretically impact the efficacy of oral contraceptives and/or estrogen replacement. Similarly, it is theoretically possible that pregnenolone could be metabolized to other steroids, resulting in hair, skin, or other steroid-related changes. Since we have determined in our prior study that pregnenolone administration does not result in downstream elevations in DHEA, DHEAS, estradiol, or testosterone, these possibilities may be unlikely;
  • Current active suicidal and/or homicidal ideation, intent, or plan;
  • Known allergy to study medication.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00728728). 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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