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Effect of epidural puncture epidural technique combined with programmed intermittent epidural bolus on breakthrough pain during delivery : a randomized controlled trial

Effect of epidural puncture epidural technique combined with programmed intermittent epidural bolus on breakthrough pain during delivery : a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078184
Enrollment
Unknown
Registered
2023-11-30
Start date
2023-12-01
Completion date
Unknown
Last updated
2023-12-03

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

Conditions

None listed

Interventions

EP:epidural analgesia
DPE:Dural Puncture Epidural Technique
DDPE:double Dural Puncture Epidural Technique

Sponsors

Fujian Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: patient requests neuraxial analgesia; nulliparous with ASA physical status 2 or 3; term pregnancy; active labour; cervical dilatation 50 (visual analogue scale (VAS);

Exclusion criteria

Exclusion criteria: known allergies to study drugs; contraindication to neuraxial anaesthesia; age < 18y;pregnancy-related diseases (ie, gestational diabetes,gestational hypertension, and preeclampsia);history of drug abuse;History of chronic pain;conditions that increase the risk of a cesarean deliv-ery (ie, placenta previa, history of uterine anomaly, or surgery)and known fetal abnormalities;Participants were also excluded from the analysis in the event of an inadvertent dural puncture using the epidural needle, when cerebrospinal fluid (CSF) could not be confirmed with the spinal needle while performing the dural puncture, or if a delivery occurred within 1 hour after epidural catheter placement.

Design outcomes

Primary

MeasureTime frame
Incidence of breakthrough pain;Adequate analgesia time;

Secondary

MeasureTime frame
maternal satisfaction;The time of the first PCEA require;Anesthetic consumption;adverse reaction;

Countries

China

Contacts

Public ContactYuanbiao Chen

Fujian Maternal and Child Health Hospital

yuanbiao1991@163.com+86 180 6084 6627

Outcome results

None listed

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