Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Clinical Trial

Long-Term Study of CartiPRO for Knee Pain Due to Osteoarthritis or Cartilage Damage

NCT: NCT07267793 · RECRUITING

NCT IDNCT07267793
StatusRECRUITING
Start Date2025-07-03
Completion2027-06
SponsorDALIM TISSEN Co., Ltd. (INDUSTRY)
First posted
Last updated

Brief Summary

This clinical trial aims to evaluate and compare the efficacy and safety of CartiPRO, an approved intra-articular atelocollagen injection, versus Synovian injection for the relief of knee pain in patients with knee osteoarthritis. The investigational device is administered intra-articularly, with a second injection given 24 weeks after the first dose. Primary and secondary endpoints include changes in pain scores (VAS), functional assessments (WOMAC, SF-36), and safety evaluations over a 36-week period.

Frequently Asked Questions

What is Long-Term Study of CartiPRO for Knee Pain Due to Osteoarthritis or Cartilage Damage?

Long-Term Study of CartiPRO for Knee Pain Due to Osteoarthritis or Cartilage Damage is a clinical trial registered under NCT07267793. Current status: RECRUITING.

What is the status of NCT07267793?

The current status of NCT07267793 (Long-Term Study of CartiPRO for Knee Pain Due to Osteoarthritis or Cartilage Damage) is: RECRUITING.

When did Long-Term Study of CartiPRO for Knee Pain Due to Osteoarthritis or Cartilage Damage start?

Long-Term Study of CartiPRO for Knee Pain Due to Osteoarthritis or Cartilage Damage started on 2025-07-03.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.