Actively Recruiting

Phase Not Applicable
Age: 18Years - 55Years
All Genders
ID07548034

Effectiveness of Ultrasound-guided Percutaneous Needle Electrolysis Combined With Therapeutic Exercise in Femoroacetabular Impingement Syndrome: a Randomized Pilot Clinical Trial

Led by CEU San Pablo University · Updated on 2026-05-05

30

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Femoroacetabular impingement is a common cause of pain at the front of the hip, particularly affecting young and middle-aged adults. This condition results from abnormal contact between the upper thigh bone and the hip socket, which can damage soft tissues and cause discomfort. Researchers are studying whether adding a minimally invasive treatment called ultrasound-guided percutaneous electrolysis to a home exercise program helps reduce hip pain and improve function better than exercises alone. Participants will be randomly divided into two groups. One group will receive two sessions of ultrasound-guided percutaneous electrolysis targeting specific hip tissues, combined with a home exercise program focusing on hip mobility, strength, and stability, performed 3 to 4 times per week for four weeks. The other group will do the same exercise program without the electrolysis treatment. The electrolysis sessions use a fine needle and a small electrical current applied under ultrasound guidance. Participants will be evaluated at the start, after one week, and after four weeks. Researchers will measure hip pain during certain tests, hip movement range, and self-reported hip function. Safety will be monitored by recording any side effects. This five-week pilot study aims to provide early evidence on whether adding electrolysis to exercise therapy might be a safe and helpful non-surgical option for hip pain due to femoroacetabular impingement.

CONDITIONS

Brief Title

Ultrasound-guided Needle Percutaneous Electrolysis With Therapeutic Exercise in Femoroacetabular Impingement Syndrome

Who Can Participate

Age: 18Years - 55Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 55 years
  • Anterior hip pain lasting more than 3 months
  • Pain score of 4 or higher on at least one provocative hip test
  • Positive result on at least one clinical test: Straight Leg Raise, FADIR, or Hip External Rotation-Flexion-Ceiling
  • Ultrasound shows pseudofibrotic tissue near the iliopsoas tendon
  • Able to provide written informed consent
Not Eligible

You will not qualify if you...

  • Previous hip surgery
  • Moderate or severe hip osteoarthritis diagnosed by imaging
  • Neurological conditions affecting the lower limbs
  • Dominant lumbar spine problems
  • Active rheumatic or systemic inflammatory diseases
  • Contraindications to percutaneous electrolysis
  • Fear of needles (Belonephobia)

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 4 weeks

Participants perform a home-based therapeutic exercise program focused on hip mobility, gluteal strengthening, core stability, and controlled hip flexor activation. The experimental group additionally receives two sessions of ultrasound-guided percutaneous electrolysis one week apart.

Initial instruction visit and follow-up visits at 1 week and 4 weeks

Trial Site Locations

Total: 1 location

1

Fisioterapia La Moraleja

Alcobendas, Madrid, Spain, 28109

Actively Recruiting

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Research Team

G

Guillermo Gallardo López

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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