Phase
Condition
Skin Wounds
Treatment
Bupivacaine with epinephrine arm
Bupivacaine
Bupivacaine and epinephrine
Clinical Study ID
Ages > 18 Female Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
>= 18 years old
Healthy with a singleton pregnancy
English or Spanish speaking
Ongoing functioning epidural throughout the laceration repair
Multiparous or nulliparous
Ability to consent for themselves
Exclusion
Exclusion Criteria:
Underwent an operative vaginal delivery and whose vaginal delivery was complicatedby a postpartum hemorrhage
Vaginal delivery was complicated by a postpartum hemorrhage
Have multiple gestations
Complaints of non-functional epidural
Allergic to bupivacaine and/or epinephrine
Epidural was a combined spinal-epidural (CSE)
Received an epidural top-off (bolus of local anesthetic injected into the epiduralcatheter) < 3 hours from the perineal repair
Experienced extreme pain at time of study consent (pain scale score > 3 on 0-10scale)
Study Design
Study Description
Connect with a study center
Montefiore Medical Center
Bronx, New York 10467
United StatesActive - Recruiting
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