RecruitingPHASE2, PHASE3NCT05696691
Ketamine & Crisis Response Plan for Suicidal Ideation in the ED
Studying Infantile neuroaxonal dystrophy
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- The University of Texas Health Science Center at San Antonio
- Principal Investigator
- Robert De Lorenzo, MD, MSMThe University of Texas Health Science Center at San Antonio
- Intervention
- Ketamine Hydrochloride(drug)
- Enrollment
- 24 target
- Eligibility
- 18-70 years · All sexes
- Timeline
- 2023 – 2026
Study locations (1)
- University Hospital, San Antonio, Texas, United States
Collaborators
National Center for Advancing Translational Sciences (NCATS)
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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