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Not Yet Recruiting NCT07684365

Does the Volume of Medication Affect the Success of Labor Epidural Analgesia

Conditions: Labor Pain and to Reduce Pain

Sex: Female
Ages: 18 Years – 50 Years
Healthy volunteers: No
Phase: PHASE4
Enrollment: 70
Sponsor: Beth Israel Deaconess Medical Center

Summary

The purpose of this study is to evaluate whether changing the volume and concentration of a medication affects the quality of pain relief and the side effects associated with labor epidural analgesia.

Eligibility Criteria

Inclusion Criteria: * 18 years of age or older * Gestational age of 36 weeks or greater * American Society of Anesthesiology physical status 2 * Induction of labor or early labor (cervical dilation \< 6cm) * Singleton gestation * Vertex presentation Exclusion Criteria: * Preeclampsia * Receiving magnesium sulfate * Having received narcotics within 4 hours * Multiple gestation * Major fetal anomalies or demise * Previous spine surgery * Known major spine pathology * Substance use disorder

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07684365). StuddyBuddy aggregates publicly available trial information.