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Non-operative Treatment in First-time Patellar Dislocation

F

Fundacion Clinica Valle del Lili

Status

Enrolling

Conditions

Patellar Dislocation

Treatments

Other: Standard care
Other: Taping
Device: Sham taping

Study type

Interventional

Funder types

Other

Identifiers

NCT06086080
1906 (Other Identifier)

Details and patient eligibility

About

Study to evaluate the conservative treatment of patients after their first episode of primary lateral patellar dislocation. Randomized controlled trial with 2 groups: standard treatment (2-weeks with brace) followed by physical therapy, compared with knee taping and physical therapy. 1-year follow-up. Measurements include physical exam, radiographs and MRI. Outcomes: recurrence, lateral patellar tilt, functional scores, apprehension, pain.

Hypothesis: less recurrence in the knee taping group, as well as better functional scores.

Full description

Patients between 10-40 years old with first patellar dislocation are invited to participate in this conservative treatment study.

Patients are excluded if they have bilateral acute patellar dislocation, previous surgeries in the affected knee, osteochondral fracture, open patellar dislocation.

This is a randomized controlled trial with four groups of treatment:

  1. Standard treatment (2-weeks with a knee brace) and physical therapy
  2. Knee taping and physical therapy (1-week with knee brace)

Sample size: 50 patients / knees Outcomes of interest: recurrence in patellar dislocation, functional scores (Banff, Norwich), return to sport, patellar tilt

Enrollment

50 estimated patients

Sex

All

Ages

10 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with first episode of acute lateral patellar dislocation during the last 7 days.

Exclusion criteria

* Patients with acute bilateral patellar dislocation.

  • Patients with open patellar dislocation.
  • Patients with previous knee surgery in the same knee.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Double Blind

50 participants in 2 patient groups

Control group
Other group
Description:
Standard care: knee brace for 2 weeks, physical therapy, sham taping (2-weeks)
Treatment:
Device: Sham taping
Other: Standard care
Intervention group
Experimental group
Description:
Knee taping for 4-weeks, knee brace for 1 week, physical therapy
Treatment:
Other: Taping
Other: Standard care

Trial contacts and locations

1

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Central trial contact

Juan P Martinez, MD; Alejandro Gallego, MD

Data sourced from clinicaltrials.gov

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