Infrared Thermographic Imaging for Early Assessment of Epidural Block Success in Obstetric Anesthesia
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Epidural Blockade
- Sponsor
- Cook County Health
- Primary Endpoint
- Change in temperature in the lower extremities
- Status
- Withdrawn
- Last Updated
- 2 years ago
Overview
Brief Summary
The purpose of this study is to describe infrared thermographic imaging as a tool for the assessment of epidural block in obstetrics patients
Detailed 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.
Investigators
Pamela Gonzalez Sr Director Clinical Research Office
Dir Clinical Research
Cook County Health
Eligibility Criteria
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.
Outcomes
Primary Outcomes
Change in temperature in the lower extremities
Time Frame: at baseline, 5 min before the epidural blockade, during and up to 30 minutes after performing the epidural blockade
thermographic images of the lower extremities will be obtained and analyzed for thermography patterns.
Secondary Outcomes
- Epidural blockade failure(Up to 30 min after performing the epidural block)
- Successful epidural blockade(up to 30 min after performing the epidural block)
- Requirement for Epidural catheter manipulation or replacement(Up to 30 min after performing the epidural block)