Comparison of the incidence of fetal prolonged deceleration after induction of labor analgesia: dural puncture epidural versus combined spinal-epidural anesthesia (prospective non-randomized comparative study)

Comparison of the incidence of fetal prolonged deceleration after induction of labor analgesia: dural puncture epidural versus combined spinal-epidural anesthesia (prospective non-randomized comparative study) - Comparison of the incidence of fetal prolonged deceleration after induction of labor analgesia: DPE vs CSEA (non-randomized comparative study)

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000035153

Enrollment

870

Registered

2019-01-01

Start date

2018-12-20

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

pregnancy

Interventions

In the DPE(intervention)group, the dura is punctured but no medication is administered into subarachnoid space at the timing of induction of labor analgesia. Then 5ml of 0.125% levobupivacaine(2.5 mcg

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: age is 20 years old or older primipara Cervix dilation is 5cm or more at the timing of induction of labor paper based informed consent is obtained before labor starts

Exclusion criteria

Exclusion criteria: multipara abnormal cardio tocogram at the timing of induction of labor contraindication of epidural anesthesia whom research director judged not qualified as research subject

Design outcomes

Primary

Measure	Time frame
The incidence of fetal severe prolonged deceleration within 90 minutes after induction of labor analgesia	—

Secondary

Measure	Time frame
mode of delivery, evaluation of satisfaction after delivery, Apgar score, umbilical cord blood analysis	—

Countries

Japan

Contacts

Public ContactSHOKO OKAHARA

Juntendo University Hospital Anesthegiology

Shoko0719@yahoo.com03-3813-3111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026