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WithdrawnNCT04921982
Efficacy of Traumatic Memory Modification Using Memory Reconsolidation and Propranolol Among Adolescents With PTSD
Researchers are comparing Propranolol and placebo to find out how the approaches affect post-traumatic stress symptoms in young people with PTSD.
Medication studyAges 12–18France
Understand this study
What is this study about?
Researchers are comparing Propranolol and placebo to find out how the approaches affect post-traumatic stress symptoms in young people with PTSD.
Who could participate?
This study is for people with PTSD. Listed age limits: 12 years to 18 years. Other eligibility criteria apply.
- Listed locations
- Angers, France · Besançon, France and 8 more locationsSee all locations and recruitment
- Activities
- Medication described in the protocol · Placebo comparator
- Compensation
- Payment and expense reimbursement have not been verified.
What to know before participating
A point to clarify
This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?
Things to check before joining
Study start dateEstimated: October 2024
- Recruitment status
- Withdrawn
- Enrollment listed in the registry
- 0
- Sponsor
- Rennes University Hospital
- Sponsor type
- Hospital / academic medical center
- Study type
- Drug
- Intervention type
- Medication / drug
- Study phase
- Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
- Locations
- France
- Age range
- From 12 Years to 18 Years
- Official registry ID
- NCT04921982
- Official title
Show the full official title
The Efficacy of Traumatic Memory Modification Using a Memory Reconsolidation Procedure Under Propranolol Among Adolescents With Post-traumatic Stress Disorder
Recruitment & locations
WithdrawnAngers · Besançon · Bohars
7 more locations
- Colombes
- Le Havre
- Limoges
- Nantes
- Poitiers
- Rennes
- Rouen
A listed location does not confirm current availability.
Questions about this study
What is this study about?
Researchers are comparing Propranolol and placebo to find out how the approaches affect post-traumatic stress symptoms in young people with PTSD.
Who is behind this study?
The study sponsor is Rennes University Hospital, a hospital or academic medical center.
Does this study involve medication?
Yes. The study involves medication, including Propranolol and Placebo.
Who can participate?
This study is for people with PTSD. Listed age limits: 12 years to 18 years. Other eligibility criteria apply.
Is this study still recruiting?
The registry lists this study as withdrawn.
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