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Comparison of the effects of epidural injection for labor analgesia: A randomized controlled trial

Comparison of the effects of epidural injection for labor analgesia: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0004389
Enrollment
93
Registered
2019-10-28
Start date
2019-11-29
Completion date
Unknown
Last updated
2021-08-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Drug : The following drugs are administered into the spinal cavity and each epidural analgesic injection is administered through different methods. Intrathecal: 0.2% ropivacaine 1.5ml + fentanyl 20 mc

Sponsors

Samsung Medical Center
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Among parturients who are scheduled to vaginal delivery -American Society of Anesthesiologists class I. II -primipara -gestational age = 36 weeks -Single child -Cervical dilation = 5cm

Exclusion criteria

Exclusion criteria: -American Anesthesiologist Society class = III -Long-term opioids user -Patients injected intravenous opioid within 4 hours prior to labor analgesia -Patients allergic to local anesthetics -gestational age < 36 weeks -multiple gestation -multipara -Preeclampsia -Preterm Premature Rupture of Membranes -non cephalic presentation -Patients who are not suitable for nerve block as blood coagulation disorder -Patients with advanced liver disease and severe renal impairment -Patients with central nervous system disease -Cardiac disease patients -Patients taking drugs that are not suitable for anticoagulants and local anesthesia

Design outcomes

Primary

MeasureTime frame
to compare the difference in epidural analgesic consumptions used per hour to delivery among three groups

Secondary

MeasureTime frame
the difference in the amount of epidural analgesia used per hour after delivery after vaginal delivery between the manual group and Programmed intermittent epidural bolus groups.;compare the differences in the request to delivery patient conrolled epidyral analgesia ratio;compare the difference in the degree of motor nerve block between manual group and programmed intermittent epidural bolus group

Countries

Korea, Republic of

Contacts

Public ContactDoyeon Kim

Samsung Medical Center

kimdoyeon31@gmail.com+82-2-3410-2470

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026