NCT06464952

Brief Summary

Despite medical advancements, PTSD remains a major issue in Veterans1. Current treatment strategies have relatively poor adherence. In patients with PTSD and cirrhosis, there is greater cognitive impairment as well as changes in gut microbiome structure and function2,3. In addition, when there is concomitant cirrhosis, medication-related treatment options become even narrower from a safety and tolerability perspective and cognitive issues pertaining to cirrhosis could impact participation3. Changes in gut microbiome in Veterans with cirrhosis and PTSD compared to those with cirrhosis without PTSD is characterized by a greater relative expression of pathobionts and reduction in stool microbiome diversity with reduction in bacteria that produce beneficial short chain fatty acids (SCFA)2. Modulation of the gut microbiome in patients with cirrhosis and PTSD may be an important therapeutic target. In prior studies with cirrhosis alone, microbial modulation using diet, antibiotics such as rifaximin, probiotics, and fecal microbiota transplant have improved gut microbial diversity and clinical outcomes in some cases4,5. In patients with cirrhosis without PTSD and in patients with PTSD without cirrhosis there is emerging evidence regarding prebiotics and other forms of gut microbial modulation. Prebiotics are such an example6. Prebiotics are natural fibers derived from carbohydrates and can be beneficial to gut microbiota (good bacteria in the gut)6. Resistant starches (RS) are dietary fiber prebiotics found naturally in many foods including potatoes, plantains, and legumes6,7. In addition to being highly accessible, RS have been shown to be well tolerated with few adverse reactions. While no studies of RS exist in PTSD + cirrhosis patients, a meta-analysis of RS in IBD has shown RS to be an effective treatment in both animal and clinical studies where improvements in clinical remission and reduced mucosal damage were found7. However, there is insufficient data regarding patients with PTSD and cirrhosis regarding gut microbial structure and function modulation with dietary supplements such as resistant starches. These starches can improve SCFA production in elderly subjects, which could in turn affect the gut-brain axis favorably8.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
16mo left

Started Jul 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress56%
Jul 2024Sep 2027

First Submitted

Initial submission to the registry

June 13, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

June 18, 2024

Completed
1 month until next milestone

Study Start

First participant enrolled

July 31, 2024

Completed
2.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 25, 2027

Expected
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 25, 2027

Last Updated

April 9, 2026

Status Verified

April 1, 2026

Enrollment Period

2.9 years

First QC Date

June 13, 2024

Last Update Submit

April 3, 2026

Conditions

Keywords

microbiomeprebioticgut-brainliver disease

Outcome Measures

Primary Outcomes (1)

  • Gut microbiome Alpha Diversity between groups

    Shannon diversity at end of interventions between both groups

    8 weeks

Secondary Outcomes (11)

  • Gut microbiome Alpha Diversity within groups at study end

    8 weeks

  • Gut microbiome Alpha Diversity within groups at mid-study

    4 weeks

  • Serum bile acids

    8 weeks

  • Serum bile acids

    8 weeks

  • Serum short-chain fatty acid (SCFA) levels

    8 weeks

  • +6 more secondary outcomes

Study Arms (2)

Resistant potato starch

EXPERIMENTAL
Dietary Supplement: Resistant potato starch

Cellulose

ACTIVE COMPARATOR
Dietary Supplement: Powdered cellulose

Interventions

Resistant potato starchDIETARY_SUPPLEMENT

Prebiotic

Resistant potato starch
Powdered celluloseDIETARY_SUPPLEMENT

Active comparator

Cellulose

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age \>18 years
  • Ability to provide informed written consent
  • Cirrhosis diagnosis
  • Willing to comply with all study procedures and be available for the duration of the study.
  • Ability to take oral medication.
  • Willing to provide study-related samples
  • Meeting the PCL-5 definition of PTSD and have a chart diagnosis of PTSD made by a mental health provider

You may not qualify if:

  • Known SARS-CoV-2 infection in the last 60 days using medical records
  • Subjects identified as, or appearing to, lack consent capacity
  • Alcohol abuse (greater than 14 drinks per week for men and 7 drinks per week for women)
  • Active illicit drug use (marijuana is allowed)
  • Use of investigational drugs, biologics, or devices within 30 days prior to randomization.
  • Individuals who are pregnant, lactating or planning on becoming pregnant during the study
  • Diagnosed inflammatory bowel disease, Crohn's disease, or Celiac disease
  • Unstable psychiatric illness (psychosis)
  • Previous gastrointestinal surgery (colorectal surgery, gastric bypass, intestinal resection)
  • Use of other prebiotics, probiotics (including yogurt containing live probiotics), postbiotics, or other fiber supplements in the last 30 days
  • Systemic antibiotics in the last 30 days
  • Fecal microbiota transplant in the last 30 days
  • Active dysphagia
  • Allergies to any of the ingredients in assigned products
  • Use of anti-diarrheal agents, stool softeners, or immunomodulatory medications in the last 30 days.
  • +2 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hunter Holmes McGuire VA Medical Center

Richmond, Virginia, 23249, United States

RECRUITING

MeSH Terms

Conditions

FibrosisStress Disorders, Post-TraumaticLiver Diseases

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and SymptomsStress Disorders, TraumaticTrauma and Stressor Related DisordersMental DisordersDigestive System Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Masking Details
Double-blind
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: RCT in patients with cirrhosis and PTSD focused on feasibility and safety
Sponsor Type
FED
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 13, 2024

First Posted

June 18, 2024

Study Start

July 31, 2024

Primary Completion (Estimated)

June 25, 2027

Study Completion (Estimated)

September 25, 2027

Last Updated

April 9, 2026

Record last verified: 2026-04

Locations