The Efficacy of a Herbal Supplement in the Prevention of PTSD
Evaluation of the Efficacy of a Herbal Supplement in the Prevention of Treatment of Post-traumatic Stress Disorder Versus Placebo (PHYTéS Study)
Sponsor: Hôpital Universitaire Sahloul
Listed as NCT03724448, this PHASE1 trial focuses on Diagnosis, Psychiatric and Follow up and remains completed. Sponsored by Hôpital Universitaire Sahloul, it has been updated 8 times since 2018, reflecting limited change activity. Mental health research at this phase helps define safety and dosing parameters for future study.
Status Flow
Change History
8 versions recorded-
Sep 2024 — Present [monthly]
Completed PHASE1
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Jul 2024 — Sep 2024 [monthly]
Completed PHASE1
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Apr 2023 — Jul 2024 [monthly]
Completed PHASE1
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Sep 2021 — Apr 2023 [monthly]
Completed PHASE1
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Jan 2021 — Sep 2021 [monthly]
Completed PHASE1
▶ Show 3 earlier versions
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Aug 2020 — Jan 2021 [monthly]
Completed PHASE1
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Sep 2019 — Aug 2020 [monthly]
Completed PHASE1
Status: Recruiting → Completed
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Nov 2018 — Sep 2019 [monthly]
Recruiting PHASE1
First recorded
Jun 2018
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Hôpital Universitaire Sahloul
For direct contact, visit the study record on ClinicalTrials.gov .