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Effects of Treatment With ENF (Electro Neuro Feedback) in the Reduction of Post-surgical Hematoma in Patients Undergoing Hip Replacement: Evaluation With Ultrasound Method

I

I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio

Status

Unknown

Conditions

Post-surgical Hematoma, Hip Replacement , Surgery

Treatments

Other: sessions with ENF (Electro Neuro Feedback).

Study type

Observational

Funder types

Other

Identifiers

NCT05196321
ENF PTA

Details and patient eligibility

About

The study evaluates patients with clinical evidence of post-surgical hematoma / seroma after hip replacement surgery. These patients will undergo ultrasound evaluation in the 4th (+/- 2) day post surgery, in which triaxial parameters of the hematoma will be measured. This evaluation will then be repeated after 5 treatment sessions with ENF (Electro Neuro Feedback). The patient will then be subjected to evaluation scales that allow to evaluate the subjective improvement of the state of well-being after treatment ENF (Electro Neuro Feedback) generates waveforms that change automatically when the impedance of the skin changes according to a compensation algorithm, i.e. according to Feedback (Feedback). T

Enrollment

20 estimated patients

Sex

All

Ages

35 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Gender: male and female
  • Age: 35-85 years include
  • Entry into the hospital rehabilitation program lasting at least 5 days following hip replacement surgery
  • Absence in history of neurological or psychiatric disorders.
  • Signature of the Informed Consent and consent to collaborate in all the procedures of the study

Exclusion criteria

  • Presence of severe neurological / psychiatric pathologies
  • to sign the Informed Consense
  • of serious cardiological pathologies that can compromise patient safety
  • of Pace Maker or spinal cord stimulators or other subcutaneous electronic instruments
  • of active tumors in the treatment area

Trial contacts and locations

1

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Central trial contact

cristina beretta

Data sourced from clinicaltrials.gov

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