Overview
Effectiveness of Clonidine, Dexmedetomidine, and Fentanyl Adjuncts for Labor Epidural Analgesia
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2024-09-01
2024-09-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The purpose of this trial is to compare the effectiveness of labor analgesia with clonidine, dexmedetomidine, or fentanyl (standard care) adjuncts.Phase:
Early Phase 1Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Grace Lim, MD, MSTreatments:
Clonidine
Dexmedetomidine
Fentanyl
Ropivacaine
Criteria
Inclusion Criteria:- >/= 18 years of age
- American Society of Anesthesiologists (ASA) Physical Status 2 or 3
- Term pregnancy (>37 gestational weeks)
- Planning epidural labor analgesia
- Singleton pregnancy
- Vertex presentation
- Planned vaginal delivery
Exclusion Criteria:
- Pre-eclampsia with or without severe features
- New initiation of antihypertensive agent within 24 hours prior to enrollment
- Uncontrolled systemic comorbidities [i.e., diabetes, hepatic, renal or cardiac]
- Known or suspected fetal abnormalities
- Allergy to study agents
- Contra-indication to neuraxial anesthesia
- Inability to communicate or participate in study procedures