Education and Training
Blood Loss Measurement During Cesarean Delivery
The aim of this study is to assess the ability of the Triton Device to measure blood loss among women undergoing elective and non-elective cesarean delivery. This patient population often experiences significant blood loss during surgery, and measurements of surgical blood loss are often inaccurate.
Stanford is currently not accepting patients for this trial.
Stanford Investigator(s):
Eligibility
Inclusion Criteria:
- American Society of Anesthesiologists physical status class I-III
- undergoing Cesarean delivery under neuraxial anesthesia
- age between 18 and 50
- gestational age greater than or equal to 37 completed weeks
- all ethnicities
Exclusion Criteria:
- contraindication for epidural or spinal analgesia (bleeding diathesis, neuropathy,
severe scoliosis, local anesthetic allergy)
- inability to adequately understand the consent form
Ages Eligible for Study
18 Years - 50 Years
Genders Eligible for Study
Female
Not currently accepting new patients for this trial
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305
Not Recruiting