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 @ 10:20 PM
Ignite Modification Date:
2025-12-24 @ 10:20 PM
NCT ID:
NCT00709735
Eligibility Criteria:
Inclusion Criteria: Afghanistan and Iraq War veterans who have been diagnosed as having combat-related PTSD
Exclusion Criteria:
1. PTSD Checklist (PCL) score (administered at the referring site) ≤ 50;
2. Current, co-existing PTSD of non-combat origin
3. Resting systolic blood pressure \<100 mm Hg
4. Medical condition that contraindicates the administration of propranolol
5. Previous adverse reaction to, or non-compliance with, a β-adrenergic blocker
6. Presence of drugs of abuse
7. Pregnancy
8. Contraindicating psychiatric condition
9. Initiation of, or change in, psychotropic medication within the two months prior to recruitment
10. Current use of medication that may involve potentially dangerous interactions with propranolol
11. Inability to understand the study's procedures, risks, and side effects, or to otherwise give informed consent for participation
12. Does not understand English
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT00709735
Study Brief:
Protocol Section:
NCT00709735