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Not yet recruiting NCT06797960

Ultrasound Guided Intra Articular Injection of Platelet Rich Fibrin Versus Hyaluronic Acid As Means of Pain Relief in Patients with Moderate Degree Knee Osteoarthritis

Early Phase I Interventional Knee Osteoarthritis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Ultra sound guided Injection of PRF intra articularly, Intra articular injection of HA.
Who it may be relevant to
Registry conditions: Knee Osteoarthritis. Basic parameters: 45 years — 70 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

ANALGESIC EFFECT of ULTRASOUND GUIDED INTRA- ARTICULAR INJECTION of PLATELET RICH FIBRIN VERSUS INJECTION of HYALURONIC ACID in PATIENTS with MODERATE KNEE OSTEOARTHRITIS. a RANDOMIZED CONTROLLED STUDY

Overview

Randomised controlled trial

Interventions

  • Device Ultra sound guided Injection of PRF intra articularly
    Intra articular injection of PRF
  • Drug Intra articular injection of HA
    Intra articular injection of HA

Primary outcome measures

  • Pain relief as measured by VAS score [Time frame: 3 months]

Eligibility criteria

Inclusion criteria

  • ASA I, II.
  • Moderate knee osteoarthritis

Exclusion criteria

  • Neurological patients.
  • Patients with uncontrolled co morbidities

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Supportive care

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06797960 · M757

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗