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Thermographic Imaging in Epidural Anesthesia

C

Cook County Health

Status

Withdrawn

Conditions

Epidural Blockade

Treatments

Device: Thermographic imaging

Study type

Observational

Funder types

Other

Identifiers

NCT02739776
IRB# 16-012

Details and patient eligibility

About

The purpose of this study is to describe infrared thermographic imaging as a tool for the assessment of epidural block in obstetrics patients

Full description

Patients will recive standard anesthesia care for epidural placement and additionally, thermographic imaging will be obtained at baseline and up to 30 min after the epidural blockade is performed.

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Parturients in active labor requesting epidural anesthesia for normal vaginal delivery

Exclusion criteria

  • Patients with lower extremity skin disorders like active infections like cellulitis, ,dermatitis, psoriasis or connective tissue disorders like scleroderma or Raynaud's phenomenon
  • Patients with diagnosed peripheral vascular disease ,venous stasis , deep venous thrombosis.
  • Patients with Severe preeclampsia with significant lower extremity edema
  • Patient on vasoactive agents like vasodilators, calcium channels blockers.

Trial design

0 participants in 1 patient group

A
Description:
Pt receiving standard Epidural block care for vaginal delivery
Treatment:
Device: Thermographic imaging

Trial contacts and locations

0

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Central trial contact

Ahmad Abou Leila, MD; Luis Sequera Ramos, MD

Data sourced from clinicaltrials.gov

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