At a glance
ClinicalIndex Comparison RecordPhase 4Completed· 100 enrolled
Drug / intervention
Bupivacaine Hydrochloridedrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Trial to Determine the Optimal Bupivacaine Dose for Initiation of Labor Epidural Pain Relief
In Brief
A Phase 4 clinical trial evaluating Bupivacaine Hydrochloride for Labor Pain and Analgesia. Completed, enrolled 100 participants across 1 site.
Detailed Summary
To estimate the dose of bupivacaine required to achieve initial effective comfort in 90% of patients (ED90) via the epidural (DPE or EPL) technique in women undergoing labor.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsLabor Pain, Analgesia
CountriesUnited States
Collaborators--
Timeline
Phase 4CompletedFinished
20222023202420252026
Enrollment StartFeb 2021
First PostedMar 2021
Primary CompletionMar 2022
TodayJul 2026
First PostedMar 24, 2021
Enrollment StartFeb 25, 2021
Primary CompletionMar 23, 2022
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 5.3 years ago
Interventions
Bupivacaine Hydrochloridedrug
Local Anesthetic Agent