Status:
WITHDRAWN
"Loss of Resistance" Versus CompuFlo® for Epidural Placement
Lead Sponsor:
The University of Texas Health Science Center, Houston
Conditions:
Pain
Epidural Analgesia
Eligibility:
FEMALE
18-65 years
Phase:
PHASE1
PHASE2
Brief Summary
The purpose of this study is to compare how well the CompuFlo® computerized syringe pump works as compared to the traditional method of inserting an epidural (a needle placed in one's back to give pai...
Detailed Description
It is possible to utilize epidural anesthesia as the sole anesthetic technique for thoracic, abdominal, and lower extremity surgeries, as a method of postoperative pain management after surgery, and f...
Eligibility Criteria
Inclusion
- Any obstetric patient presenting for vaginal delivery desiring epidural anesthesia
- American Society of Anesthesiologists (ASA) Physical Classification I-III
- Aged 18-65 years
Exclusion
- Obstetric patients presenting for Cesarean section
- American Society of Anesthesiologists Physical Classification ≥ IV
- Contraindications for epidural anesthesia
- Allergy to local anesthetics
Key Trial Info
Start Date :
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00178750
Last Update
November 5 2020
Active Locations (1)
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1
Memorial Hermann Hospital
Houston, Texas, United States, 77030