Last updated: August 26, 2022
Sponsor: Nucleo De Pesquisa E Desenvolvimento De Medicamentos Da Universidade Federal Do Ceara
Overall Status: Completed
Phase
2/3
Condition
Psychosis
Stress
Tourette's Syndrome
Treatment
N/AClinical Study ID
NCT03788759
LipoicStudy
Ages 18-60 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Capacity to provide informed consent;
- Schizophrenia diagnosis (made by research psychiatrists using the Structured ClinicalInterview, SCID-5, for Diagnostic and Statistical Manual of Mental Disorders);
- Negative and/or cognitive symptoms despite adequate antipsychotic treatment;
- Ages 18-60 years
Exclusion
Exclusion Criteria:
- 6-month history of any drug or alcohol abuse or dependence;
- Changes in psychotropic medications within the last 4 weeks;
- Actual valproate use (potential interaction with ALA);
- General medical illness including autoimmune disorders, known chronic infections suchas HIV or hepatitis C, and liver or renal failure that could adversely impact onpatient outcome;
- Women who are planning to become pregnant, are pregnant, or are breastfeeding.
Study Design
Total Participants: 48
Study Start date:
September 01, 2019
Estimated Completion Date:
December 01, 2021
Study Description
Connect with a study center
Núcleo de Pesquisa e Desenvolvimento de Medicamentos - UFC
Fortaleza, CE 60430-275
BrazilSite Not Available
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