Status:

UNKNOWN

Evaluation of the Recovery of the Sympathetic Block After Spinal Anesthesia by Thermographic Image

Lead Sponsor:

Central Hospital, Nancy, France

Conditions:

Spinal Anesthesia

Eligibility:

All Genders

18+ years

Brief Summary

Spinal anesthesia is a locoregional perimedullary anesthesia which consists of temporary interruption of nerve transmission within the subarachnoid space. This anesthesia is produced, via a lumbar pu...

Detailed Description

Main objective is the following: To evaluate the performance of thermography to assess the state of total recovery of the sympathetic block after spinal anesthesia, the evolution of hemodynamic param...

Eligibility Criteria

Inclusion

  • Person who has received complete information on the organization of the research and has not opposed their participation and the use of their data
  • Adult patients,
  • ASA score from I to 3 stabilized
  • Outpatient orthopedic surgery of the lower limbs scheduled at the CCEG-Regional University Hospital Center of NANCY
  • Locoregional anesthesia by spinal anesthesia
  • Affiliation to a social security scheme or beneficiary of such a scheme

Exclusion

  • Documented allergy to one of the agents injected intrathecally
  • Uncorrected absolute and / or relative hypovolaemia, as well as situations where the hemodynamics are not stabilized (state of shock, cardiac decompensation, etc.)
  • Obstructive heart disease (tight mitral stenosis, tight aortic stenosis, obstructive hypertrophic cardiomyopathy)
  • Arterial hypertension uncontrolled
  • Constrictive pericarditis
  • Obliterating arterial disease of the lower limbs
  • Raynaud's syndrome
  • Localized infection near the puncture site and / or documented systemic infection
  • Infection of the lower limbs like erysipelas
  • Hemostatic disorder
  • Intracranial hypertension
  • Neurodegenerative diseases of the spinal cord
  • Congenital malformations (spina bifida)
  • Surgical emergency
  • Multi visceral failure
  • Conventional hospitalization
  • Persons referred to in Articles L. 1121-5 to L. 1121-8 and L1122-2 of the Public Health Code:
  • Pregnant woman, parturient or nursing mother
  • Person deprived of liberty by a judicial or administrative decision
  • Person unable to express their consent
  • Person undergoing psychiatric treatment under Articles L. 3212-1 and L. 3213-1 of the Public Health Code
  • Minor (not emancipated)
  • Adult person subject to a legal protection measure (guardianship, curatorship, safeguard of justice)

Key Trial Info

Start Date :

March 1 2022

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

April 1 2023

Estimated Enrollment :

63 Patients enrolled

Trial Details

Trial ID

NCT05277220

Start Date

March 1 2022

End Date

April 1 2023

Last Update

March 14 2022

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