Ginger and the Microbiota-gut-brain Connection in Sciatic Pain Individuals

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug, Dietary supplement
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Neuropathic pain affects the quality of life of many Americans. Non-pharmacological strategies such as bioactive compounds in foods are being explored as therapeutics but can also serve as tools to better understand pain mechanisms. The previous study reported that ginger root extract supplementation palliated pain-spectrum behaviors in animals with neuropathic pain via the microbiota-gut-brain axis. The proposed study is primarily designed to use ginger supplementation for a better understanding of the role of microbiota-gut-brain interactions in sciatica states in a randomized, double-blinded, and placebo-controlled trial. Eighty participants with sciatica will be randomized to receive placebo (2000 mg starch daily) or ginger (2000 mg daily) for 8 weeks. This study will evaluate the effects of ginger supplementation on gut function measured as gut microbiota composition using 16S rRNA sequencing analysis, intestinal permeability based on plasma lipopolysaccharide binding protein and fecal zonulin using ELISA, and fecal metabolites using LC-MS/MS analysis (SA 1); on neuroinflammation in whole blood mRNA using nCounter® Neuroinflammation Panels analysis (SA 2); and on pain-associated outcomes and brain neuroplasticity by assessing functional (resting state-fMRI) and structural (Diffusion Tensor Imaging) connectivity (SA 3).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
View:

• 18-85 years old men and women with BMI \< 25 or ≥ 30 kg/m2

• low back or gluteal pain radiating into leg(s) past the knee (sciatica) with pain duration of at least 3 months (chronic sciatica)

• pain scale \> 3 out of 10 (0=no pain,10=worst pain imaginable) during the past 24 hours

• willingness to accept randomization.

• woman of childbearing potential agrees to use an effective form of contraception during the study

Locations
United States
Texas
Texas Tech University Health Sciences Center
RECRUITING
Lubbock
Texas Tech University Health Sciences Center
NOT_YET_RECRUITING
Lubbock
Contact Information
Primary
Chwan-Li (Leslie) Shen, PhD
leslie.shen@ttuhsc.edu
806-743-2815
Time Frame
Start Date: 2025-07-01
Estimated Completion Date: 2028-02-28
Participants
Target number of participants: 80
Treatments
Placebo_comparator: Placebo
Placebo group: 2,000 mg cellulose daily for 8 weeks
Active_comparator: Ginger
Ginger group: 2,000 mg ginger root extract daily for 8 weeks
Sponsors
Leads: Leslie Shen

This content was sourced from clinicaltrials.gov