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Probiotic Supplements in Osteoarthritis

NCT07364578 · Status: RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 146

Last updated 2026-01-30

No results posted yet for this study

Summary

The current study aims to evaluate the effectiveness of adding probiotics to the standard of care in improving OA patient-related outcomes such as pain, stiffness, and physical activity.

Conditions

  • Osteoarthritis, Knee

Interventions

DRUG

Probiotic Formula

probiotic supplements (lactobacillus, 2 times daily) added to standard of care

DRUG

Control

standard of care

Sponsors & Collaborators

  • Beni-Suef University

    lead OTHER

Principal Investigators

  • Asmaa Elsayed · Beni-Suef University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-02-15
Primary Completion
2026-02-15
Completion
2026-03-01

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07364578 on ClinicalTrials.gov