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NCT05508815

Modified Zhiwang Decoction Combined With Methotrexate in the Treatment of Early Rheumatoid Arthritis

Status unknown EARLY_PHASE1 Last updated 25 May 2023
What this trial tests

EARLY_PHASE1 trial testing Modified Zhiwang Decoction Combined with methotrexate in Arthritis, Rheumatoid in 150 participants. Status unknown.

Timeline
9 February 2023
Primary endpoint
31 December 2024
31 December 2024

Quick facts

Lead sponsorBeijing University of Chinese Medicine
PhaseEARLY_PHASE1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment150
Start date9 February 2023
Primary completion31 December 2024
Estimated completion31 December 2024
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Beijing University of Chinese Medicine

Who can join

Adults 16 to 70, any sex, with Arthritis, Rheumatoid. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study is to evaluate the effectiveness and safety of Modified Zhiwang Decoction in combination with methotrexate for the treatment of early RA patients and a parallel-group, single-center randomized controlled clinical study was designed.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Efficacy and safety of the modified Zhiwang decoction combined with methotrexate in early rheumatoid arthritis: study protocol for a randomised controlled trial.
    Zhang N, Zhang LB, Wang Z, Lan TY, et al · · 2024 · cited 2× · PMID 38238175 · DOI 10.1136/bmjopen-2023-076571

Verify or expand the search:

Other recruiting trials for Arthritis, Rheumatoid

Currently open trials in the same condition.

Other Beijing University of Chinese Medicine trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05508815.

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