Sentra AM® and Sentra PM® for Post-traumatic Stress Disorder (PTSD) and Gulf War Fibromyalgia (GWF)

An Open-label Clinical Outcomes Study to Determine the Safety and Efficacy of Sentra AM® and Sentra PM® for Post-traumatic Stress Disorder and Gulf War Fibromyalgia

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01437891

Acronym

GWF001

Enrollment

Registered

2011-09-21

Start date

2011-09-30

Completion date

2012-01-31

Last updated

2012-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Persian Gulf Syndrome, Post-traumatic Stress Disorder

Keywords

PTSD, Military veteran, Gulf War, Fibromyalgia, Gulf War Syndrome

Brief summary

An open-label clinical outcomes study to determine the safety and efficacy of Sentra AM® and Sentra PM® for post-traumatic stress disorder (PTSD) and Gulf War fibromyalgia (GWF).

Detailed description

Male and female military veterans age 18 to 75 experiencing moderate to severe PTSD symptoms including cognitive dysfunction, sleep disorders and mood disorders. Open-label internet questionnaire-based clinical outcomes study. 250 subjects. 60 days from enrollment initiation to completion and study close. Sentra AM- two capsules given orally once daily in the morning for 30 days. Sentra PM- two capsules given orally once daily thirty minutes before bedtime for 30 days. To measure improvement in quality of life determined by the change in short form-36 (SF-36) general health survey. Improvements in daytime sleepiness determined by the Epworth Sleepiness Scale (ESS), improvement in cognitive and emotional function using the Cognitive emotion regulation questionnaire - short (CERQ-Short), change in PTSD symptoms with the Primary Care - PTSD (PC-PTSD), Psychopathy Checklist- Military (PCL-M). Heart rate variability (HRV) data variation will be measured in a group of twenty subjects.

Interventions

None listed

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 75 Years

Healthy volunteers

Inclusion criteria

1. United States military veterans reporting PTSD and/or Gulf War Illness symptoms at least three months after return from duty. 2. Men and non-pregnant, non-lactating women over the age of 18 and under the age of 75, able to read and understand English-language informed consent. 3. Men and women of child-bearing potential willing to use adequate contraception, not to become pregnant or impregnate their partner for the study duration. 4. Patients who will continue on a stable dose (no less than three months) of other medications they are taking and maintain the same dose throughout the duration of the study. 5. Patients willing to commit to completing all clinical questionnaires and guidelines during study-related procedures.

Exclusion criteria

1. Patients who have previously taken Sentra AM or Sentra PM. 2. Patients not fluent in English. 3. Participation in a clinical trial within one (1) month prior to screening. 4. Uncontrolled or unstable serious cardiovascular, pulmonary, gastrointestinal, endocrine or neurologic disorder.

Design outcomes

Primary

Measure	Time frame	Description
SF-36 general health survey	Baseline and Day 30	A general health questionnaire to measure quality of life. Change from baseline.

Secondary

Measure	Time frame	Description
Epworth Sleepiness Scale	Baseline and Day 30	Improvements in daytime sleepiness determined by the Epworth Sleepiness Scale.
CERQ-short	Baseline and Day 30	Assessment of cognitive function. Change from baseline.
PCL-Military	Baseline and Day 30	Changes in symptoms of military specific PTSD.

Countries

United States

Outcome results