CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 30 enrolled
Drug / intervention
Eco-guided Triamcinolone-Acetonide injectionprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04943341
NCT04943341N/ACompleted

Eco-guided Treatment With Triamcinolone-Acetonide in the Treatment of Medial Plica Syndrome - A Pilot Study

Istituto Ortopedico Rizzoli·interventional·Posted Jun 29, 2021·Updated Nov 18, 2025

In Brief

A clinical study evaluating Eco-guided Triamcinolone-Acetonide injection for Medial Plica Syndrome. Completed, enrolled 30 participants across 1 site.

Detailed Summary

The aim of this pilot study is to evaluate the clinical and radiological outcomes (ultrasound and MRI) for a treatment utilized in the medial plica syndrome resistant to conservative therapy. Will be evaluated an intra-plica ultrasound-guided injections of Triamcinolone-Acetonide and lidocaine percutaneously, and associated rehabilitation therapy. The aim of the study will be to evaluate the efficacy and safety of the injection procedure by revealing clinical improvement and monitoring the incidence of adverse events following treatment.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesItaly
Collaborators--

Timeline

N/ACompletedFinished
20222023202420252026
First PostedJun 29, 2021
Enrollment StartOct 28, 2021
Primary CompletionSep 16, 2024
Study CompletionSep 30, 2025
TodayJul 2, 2026
Enrollment to primary: 2.9 yearsPosted 5.0 years ago

Interventions

Eco-guided Triamcinolone-Acetonide injectionprocedure

The treatment consists in injecting 1 ml of Kenacort (corresponding to 40 mg of Triamcinolone Acetonide) diluted in about 1 ml of local anesthetic (Lidocaine) directly into the medial fold of the knee. Through an ultrasound guidance with "in plane" technique, the flute beak of the needle will be positioned between the two sheets of the synovial fold and the injection will be performed.