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Study ID: NCT00648375. We help you review the study, but cannot decide medical eligibility.
TerminatedNCT00648375
Effectiveness of Propranolol For Treating People With PTSD
This study has public registry information. It focuses on PTSD and currently lists study information in the United States.
PTSDBehavioralFrom 18 Years to 50 Years
Understand this study
Who could participate?
Listed age limits: 18 years to 50 years.
- Listed locations
- New York, United StatesSee all locations and recruitment
Compensation and expense reimbursement have not been verified for this summary.
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 dateDecember 2003
- Recruitment status
- Terminated
- Enrollment listed in the registry
- 12
- Sponsor
- Weill Medical College of Cornell University
- Sponsor type
- University
- Study type
- Behavioral
- Intervention type
- Psychotherapy / behavioral intervention, Medication / drug
- Study phase
- Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
- Locations
- United States
- Age range
- From 18 Years to 50 Years
- Official registry ID
- NCT00648375
- Official title
- Efficacy of Propanolol for Treatment of Posttraumatic Stress Disorder
Recruitment & locations
TerminatedNew York
A listed location does not confirm current availability.
Questions about this study
Who is behind this study?
The study sponsor is Weill Medical College of Cornell University, a university.
Does this study involve medication?
Yes. The study involves medication, including Propanolol and Placebo.
Who can participate?
Listed age limits: 18 years to 50 years.
Is this study still recruiting?
The registry lists this study as terminated.
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