Complex Regional Pain Syndrome Clinical Trials

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Role of the Gut Microbiome in Complex Regional Pain Syndrome

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The objective of this prospective, observational study is to determine the association between the composition of the gut microbiota and the severity and persistence of Complex Regional Pain Syndrome symptoms (Study A). The objective of Study B, a longitudinal study of microbiota biomarkers of patients with newly diagnosed CRPS is to determine if the researchers can predict which patients are more likely to recover compared to those who do not. A secondary objective of both studies is to examine cognitive flexibility in relation to outcomes (study A and B).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Adults over the age of 18

• Current (\< 1 year duration) or former (\> 1 year) diagnosis of Complex Regional Pain Syndrome by the Budapest criteria

• English as primary language

• able to consent

• Adults over age of 18

• Cohabitant of person with current or former diagnosis of CRPS

⁃ Study B: Longitudinal Study

• Adults over the age of 18

• Recent diagnosis (\<6 months) of Complex Regional Pain Syndrome by the Budapest criteria

• English as primary language

• able to consent

• Adults over age of 18

• Cohabitant of person with diagnosis of CRPS

Locations
United States
Missouri
Washington University School of Medicine
RECRUITING
St Louis
Contact Information
Primary
Lara Crock, MD PhD
crockl@wustl.edu
314-546-3882
Time Frame
Start Date: 2018-12-19
Estimated Completion Date: 2027-07
Participants
Target number of participants: 140
Treatments
Study A: Chronic >1 year
Study A: Acute <1 year
Study A: Household Control
Study B: Newly Diagnosed <6 months
Study B: Household Controls
Related Therapeutic Areas
Sponsors
Leads: Washington University School of Medicine

This content was sourced from clinicaltrials.gov