Active — Not RecruitingNot Applicable

A Confirmatory Trial of Multidisciplinary Digital Therapeutics for Patellofemoral Pain Syndrome

South Korea216 participantsStarted 2024-04-26

Plain-language summary

This randomized controlled confirmatory study will be evaluating an mobile application, MORA Cure (ETH-01K), owned by EverEx, Inc., to examine safety and effectiveness in individuals with patellofemoral pain syndrome.

Who can participate

SexALL

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Inclusion criteria

✓. Patients with peripatellar or posterior patellar pain in one or more knee joints for 3 months or longer
✓. Patients with peripatellar or posterior patellar pain provoked by squatting
✓. Patients who have pain provoked by 2 or more following activities: prolonged sitting, cycling, running, going up or down stairs, kneeling, compression of the patella, palpation of the patellar facets
✓. Patients who signed a written informed consent form

Exclusion criteria

✕. Patients with osteoarthritis which scored 3 or higher grade of the Kellgren-Lawrence scale
✕. Patients diagnosed with a fracture or dislocation around the knee within the last 3 months
✕. Patients who had knee surgery within the last 3 months
✕. Patients diagnosed with patellar tendinitis based on imaging within 3 months
✕. Patients taking narcotic pain medications for pain control
✕. Patients taking or planning to take any medication that is a contraindication within the next 16 weeks at the time of screening
✕. Patients who are pregnant
✕. Patients currently participating in another clinical trial or have participated in another clinical trial within the past 3 months at the time of screening

What they're measuring

Usual pain severity assessed by the Visual Analogue Scale (VAS)

Timeframe: 8 weeks

Trial details

NCT IDNCT06260865

SponsorEverEx Inc.

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2025-03-31

View on ClinicalTrials.gov More Patellofemoral Pain Syndrome trials