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Efficacy and Safety of Dural Puncture Epidural Anesthesia with Double-orifice Epidural Catheter Combined with Programmed Intermittent Epidural Bolus in Labor Analgesia

Efficacy and Safety of Dural Puncture Epidural Anesthesia with Double-orifice Epidural Catheter Combined with Programmed Intermittent Epidural Bolus in Labor Analgesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120022
Enrollment
Unknown
Registered
2026-03-09
Start date
2026-03-31
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

None

Interventions

Test Group:A small hole was made at 4 cm of the epidural catheter, and after dural puncture epidural anesthesia at L2-3, the epidural catheter was inserted 4 cm.
Control Group:After dural puncture epidural anesthesia at L2-3, the epidural catheter was inserted 4 cm.

Sponsors

Maternal and Child Health Hospital of Jiangxi Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Full-term (37 weeks of gestation or more) primiparas with a single cephalic presentation. 2. American Society of Anesthesiologists (ASA) classification of grade II. 3. Cervical dilation less than 5 cm, no obvious obstetric complications, and no contraindications to natural vaginal delivery.

Exclusion criteria

Exclusion criteria: 1. The parturient refused to participate in this study. 2. There are contraindications for intrathecal anesthesia, including allergy to anesthetic drugs, abnormal coagulation function, spinal deformity, severe hypovolemia or unstable hemodynamics. 3. High-risk pregnancies, such as placenta previa, preeclampsia, etc. 4. Having a history of chronic pain, or long-term use of analgesics, sedatives, antidepressants. 5. Presence of communication disorders, history of mental illness, poor mood or epilepsy. 6. The parturient was unable to cooperate with the study or could not undergo the interview.

Design outcomes

Primary

MeasureTime frame
Time to achieve adequate analgesia (Visual Analog Scale, VAS =3) with dural puncture epidural anesthesia.;

Secondary

MeasureTime frame
VAS pain score at 10 minutes before the procedure.;VAS pain score at 10 minutes after the procedure.;VAS pain score at 20 minutes after the procedure.;VAS pain score at 30 minutes after the procedure.;VAS pain score when the cervix is fully dilated (T4);Patient Satisfaction Score;Total number of requests for PCEA pump;Total drug consumption of PCEA pump;

Countries

China

Contacts

Public ContactJingzi Rao

Jiangxi Maternal and Child Health Hospital

2856550975@qq.com+86 187 2099 7945

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026