Overview

Effectiveness of Clonidine, Dexmedetomidine, and Fentanyl Adjuncts for Labor Epidural Analgesia

Status:
Not yet recruiting
Trial end date:
2024-09-01
Target enrollment:
0
Participant gender:
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 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Grace Lim, MD, MS
Treatments:
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