Rush University Medical Center
Chicago, Illinois, 60612, United States
NCT Number: NCT06643299
The goal of this clinical trial is to learn if probiotics can improve symptoms and quality of life in participants with Long COVID.
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Notify Me18 year and older
All sexes
Interventional
Phase 2
Chicago, Illinois, 60612, United States
The goal of this clinical trial is to learn if probiotics can improve symptoms and quality of life in participants with Long COVID. The main questions it aims to answer are:
Researchers will compare probiotics to a placebo (a look-alike substance that contains no probiotics) to see if probiotics work to treat Long COVID.
Participants will take the study medication (placebo or probiotic) for 4 months. They will then cross over (take the other medication) for an additional 4 months. Participants will complete a survey at baseline, 4 months, and 8 months.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
BlueBiology: Ultimate Care probiotic pill taken once daily for a four-month period.
Other names: BlueBiotics: Ultimate Care
Placebo produced to be identical in taste and appearance to the probiotic agent, taken once daily for a four-month period.
Time frame: Baseline, Four, and Eight Months
Defined as the percentage change from moderate-to-severe Long COVID to mild Long COVID using the Long COVID Symptoms and Severity Score (LC-SSS) tool between groups with subgroup analysis by Long COVID trajectory
Time frame: Baseline, Four, and Eight Months
Defined as the change in the LC-SSS total score between groups with subgroup analysis by individual symptom scores and Long COVID trajectory
Time frame: Baseline, Four, and Eight Months
Defined as the change in score for PROMIS-29 physical and mental health and the PROMIS SF-Cognitive Function 8a scale between groups with subgroup analysis by Long COVID trajectory
Time frame: Baseline, Four, and Eight Months
Defined as the change in the Work Productivity and Activity Impairment tool scores between groups with subgroup analysis by Long COVID trajectory
Rush University Medical Center
Other
PURE-LC - Probiotic Use for Recovery Enhancement From Long COVID
Acronym: PURE-LC
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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