Tong-Luo-Qu-Tong Plaster for KOA: a Randomised, Double-blind, Parallel Positive Control, Multi-center Clinical Trial

NCT03309501 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 2000

Last updated 2017-11-09

No results posted yet for this study

Summary

Knee osteoarthritis(OA), also known as degenerative arthritis, have affected a lot of people. Patients with severe osteoarthritis frequently develop one or more of the typically following symptoms: joint pain, stiffness, activity with joint friction noise, limited mobility, such as difficulty walking and climbing. Now there are many western medicine treatments including symptom relief and joint cartilage protective agents for OA, but the results have not yet satisfied. TCM treatment of osteoarthritis has remarkable curative effect and unique advantage.Tong-Luo-Qu-Tong Plaster is a common method to treat osteoarthritis of the knee for thousands of years in China. It lacked a large sample randomised, double-blind, parallel positive controlled, multicenter clinical trial, and the clinical evidence of Tong-Luo-Qu-Tong Plaster for Knee Osteoarthritis need to be further completed.

Conditions

Interventions

DRUG

Tong-Luo-Qu-Tong Plaster

for 14 days as two period of treatment, daily 1 time.

DRUG

Qi-Zheng-Xiao-Tong Plaster

for 14 days as two period of treatment, daily 1 time

Sponsors & Collaborators

  • Shanghai Zhongshan Hospital

    collaborator OTHER
  • Suzhou Hospital of Traditional Chinese Medicine

    collaborator OTHER
  • Luoyang Osteopathy hospital of Henan

    collaborator UNKNOWN
  • Hubei Hospital of Traditional Chinese Medicine

    collaborator OTHER
  • Liaoning University of Traditional Chinese Medicine

    collaborator OTHER
  • The Second Hospital of Nanjing Medical University

    collaborator OTHER
  • The Fourth Central Hospital of Tianjin

    collaborator UNKNOWN
  • Shanghai University of Traditional Chinese Medicine

    lead OTHER

Principal Investigators

  • Yongjun Wang, Doctor · Longhua Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-09-12
Primary Completion
2019-12-20
Completion
2020-09-20

Countries

  • China

Study Locations

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Entities

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 NCT03309501 on ClinicalTrials.gov