Effect of Lower Extremity Traction on the Popliteal Angle After Percutaneous Needle Tenotomy of the Knee Flexor Muscles.

Last updated: March 2, 2023
Sponsor: Institut de Sante Parasport Connecte Synergies
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

N/A

Clinical Study ID

NCT05736328
2023-002
  • Ages > 18
  • All Genders

Study Summary

People with neuromotor disability (i.e. following an inborn or acquired spinal cord, cerebral or peripheral neurological lesion) are at risk of neuro-orthopaedic disorders. Microinvasive percutaneous needle tenotomy is a frequent use alternative to open surgery to treat limb deformities. A lower extremity traction is performed in our unit during 2 to 7 days after surgery of the knee flexor muscles.

The aim of this study is to describe the efficiency of lower extremity traction on the popliteal angle after percutaneous needle tenotomy of the knee flexor muscles.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients >= 18 years old ;
  • Treated in the Perioperative Disability Unit (UPOH) of the Physical Medicine andRehabilitation Department of our university hospital;
  • Admitted for the treatment of limb deformities by percutaneous needle tenotomy of theknee flexor muscles ;
  • Having a neuromotor disability;
  • No opposition to be enrolled in the study from the patient, or from a legallyauthorized close relative if the patient's state of health does not allow it;
  • Affiliation to a social security scheme.

Exclusion

Exclusion Criteria:

  • Associated open surgery ;
  • Associated bone surgery ;
  • Under court protection.

Study Design

Total Participants: 20
Study Start date:
March 02, 2023
Estimated Completion Date:
February 28, 2024

Study Description

This is a prospective, monocentric, cohort study of neurological disabled inpatients subjects treated in the perioperative disability unit (UPOH) of our university hospital for limb deformities by percutaneous needle tenotomy of the knee flexor muscles.

All eligible inpatient subjects with neuromotor disability and admitted for the treatment of limb deformities by percutaneous needle tenotomy of the knee flexor muscles will be consecutively included.

Data will be collected from the patients' medical records, in particular data related to their clinical, radiological, biological, and physiological examinations.

This is a routine care study; no procedures are added for research purposes. It is an ancillary study to the NO-AGING study.

Connect with a study center

  • Department of Physical Medicine and Rehabilitation, Raymond Poincaré Hospital, AP-HP

    Garches, 92380
    France

    Active - Recruiting

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