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NCT03734900

Comparison of Effectiveness Between PL and PRP on Knee Osteoarthritis: a Prospective,Randomized,Placebo-controlled Trial

Status unknown Phase 4 Last updated 20 September 2021
What this trial tests

Phase 4 trial testing Saline injection in Osteoarthritis (OA) of the Knee in 150 participants. Status unknown.

Timeline
15 May 2018
Primary endpoint
14 May 2022
14 May 2022

Quick facts

Lead sponsorNational Taiwan University Hospital
PhasePhase 4
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment150
Start date15 May 2018
Primary completion14 May 2022
Estimated completion14 May 2022
Sites1 location across Taiwan

Drugs / interventions tested

Conditions studied

Sponsor

National Taiwan University Hospital

Who can join

Adults 50 to 80, any sex, with Osteoarthritis (OA) of the Knee. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will focus on grade I to III knee osteoarthritis by randomized controlled trials which comparing the effectiveness between placebo, autologous platelet rich plasma and autologous platelet lysate injections.

Publications & conference data

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

  1. Platelet Lysate and Osteoarthritis of the Knee: A Review of Current Clinical Evidence.
    Gupta A, Maffulli N. · · 2024 · cited 10× · PMID 39340713 · DOI 10.1007/s40122-024-00661-y

Verify or expand the search:

Other trials of Saline injection

Trials testing the same drug.

Other recruiting trials for Osteoarthritis (OA) of the Knee

Currently open trials in the same condition.

Other National Taiwan University Hospital 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/NCT03734900.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing