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Not Yet Recruiting NCT05743543

A Pilot Study of SPG Block for PTSD

Conditions: Post Traumatic Stress Disorder

Sex: All
Ages: 18 Years – 60 Years
Phase: EARLY_PHASE1
Enrollment: 20
Sponsor: New York State Psychiatric Institute

Summary

Some patients with Post Traumatic Stress Disorder (PTSD) respond only partially to medication. This study is a pilot study investigating whether blocking the SPG helps reduce the symptoms of PTSD. This study does not involve treatment with medications. It is a proof of principal study.

Eligibility Criteria

Inclusion Criteria:Participants with a principal diagnosis of PTSD on stable dose of psychiatric medication or in stable psychotherapy for at least 3 months, who experience residual symptoms.Participants who understand all study procedures and can undergo informed consentExclusion Criteria:Participants with a medical disorder, for whom study participation could be deleterious (neurologic, cardiac, renal or infectious disease)Pregnant or breast feeding participantsParticipants who are on an anticoagulant, such as warfarin, or otherwise have a medical condition that increases bleeding risk

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05743543). StuddyBuddy aggregates publicly available trial information.