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Transcutaneous Oxygen Pressure of the Injured Ankle as Predictor of Postoperative Cutaneous Pain (TAC)

N

Nantes University Hospital (NUH)

Status

Completed

Conditions

Ankle Injuries

Treatments

Device: measurement of TcPO2 with skin electrode

Study type

Observational

Funder types

Other

Identifiers

NCT04209582
RC19_0303

Details and patient eligibility

About

This monocentric prospective observational pilot study aims to investigate if the measurement of TcPO2 can be used as a predictor of postoperative cutaneous pain in patients with ankle surgery.

Full description

This prospective observational study aims to determine the limit of TcPO2 predictive of postoperative cutaneous pain in patients with ankle trauma.

A TcPO2 measurement will be performed preoperatively at the patient's arrival in the emergency room, then every day after the operation for 3 days and finally at the follow-up visits at 3 and 6 weeks.

The cutaneous pain is evaluated by a PSAS self-questionnaire (completed by the patient) and an OSAS questionnaire (completed by the surgeon). These grids evaluate the tolerance and cicatricial quality in the medium and long term by the operator and the patient.

Enrollment

39 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with surgery of ankle trauma

Exclusion criteria

  • Patient who does not agree to participate
  • Patient unable to express agreement (ex: unconscious)
  • Minor patient
  • Major patient under tutorship or curatorship

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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