Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:28 PM
Ignite Modification Date:
2025-12-24 @ 11:28 PM
NCT ID:
NCT01713556
Eligibility Criteria:
Inclusion Criteria:
* Diagnosis of chronic PTSD
* PTSD CheckList total score \>44
Exclusion Criteria:
* Systolic blood pressure \< 100 mmHg
* Contraindication to Propranolol
* Previous adverse reaction to a β-blocker
* Use of another β-blocker
* Use of medication that could involve potentially dangerous interactions with propranolol
* Psychotherapy or treatment with any pharmacologic PTSD medication within the 2 weeks prior to inclusion (6 weeks for fluoxetine)
* Female with reproductive potential without reliable means of contraception
* Pregnancy or lactation
* Alcohol or drug abuse
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT01713556
Study Brief:
Protocol Section:
NCT01713556