drugset / Trial / NCT05576597

Effect of Butyrate Supplement on Rheumatoid Arthritis

NCT05576597 ↗

Phase 2 Completed 30 enrolled Peking University People's Hospital
NaSingle-groupOpen-labelTreatment

Summary

This study is a pilot study to evaluate the safety and efficacy of administering butyrate supplement on rheumatoid arthritis patients. Thirty participants will be included to receive butyrate supplement for 12 weeks. Changes of immune cell subtypes, markers of intestinal damage, intestinal flora and other laboratory indicators will be monitored.

Timeline

Start
2022-08-23
Primary completion
2023-10-01
Completion
2024-06-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Sodium Butyrate Small molecule 1200 mg —

Indications