Clinical Trials Directory

Trials / Completed

CompletedNCT07472777

Long-term Efficacy of Modified Guilu Erxian Glue for Myasthenia Gravis

Long-term Efficacy of Modified Guilu Erxian Glue in Treating Patients With Myasthenia Gravis: A Retrospective Cohort Study

Status
Completed
Phase
Study type
Observational
Enrollment
231 (actual)
Sponsor
Beijing University of Chinese Medicine · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Through a retrospective cohort study method, the influence of Gu-Lu Er-Xian Decoction with modified formula on the long-term therapeutic effect of patients with myasthenia gravis was analyzed, and the related factors affecting recurrence were also explored.

Detailed description

Screen the medical records of MG patients who visited the hospital from January 2020 to January 2024. By July 31, 2024, the final follow-up for the patient outcomes was completed. Taking the cumulative use of Gui鹿 Erxian Jiawo Formula for ≥ 1 month per year as the exposure factor, the included patients were divided into the exposure group and the non-exposure group. The clinical characteristics and medium-to-long-term efficacy of the two groups were compared. The primary outcome was the recurrence rate, and the secondary outcomes included the time for the first reduction of conventional Western medicine dosage, MGFA classification, GFA-PIS, TCM syndrome score, HAMA, the incidence of myasthenic crisis, and MG-ADL. Through Cox multivariate regression analysis, the factors related to MG recurrence were analyzed.

Conditions

Timeline

Start date
2024-01-01
Primary completion
2024-07-31
Completion
2024-07-31
First posted
2026-03-16
Last updated
2026-03-16

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07472777. Inclusion in this directory is not an endorsement.