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Effect of Dural Puncture Epidural Technique with Programmed Intermittent Bolus on Labor Analgesia

Effect of Dural Puncture Epidural Technique with Programmed Intermittent Bolus on Labor Analgesia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900024717
Enrollment
Unknown
Registered
2019-07-23
Start date
2019-09-02
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Labor Analgesia

Interventions

DPE group:Dural Puncture with 25G spinal needle
EA group:without Dural Puncture

Sponsors

The First Affiliated Hospital of Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Primigravida parturients of ASA grade I and II with uncomplicated pregnancy in vertex presentation at 38 to 42 weeks gestation in active labor with cervical dilatation 3~5.0 cm and desiring epidural labor analgesia.

Exclusion criteria

Exclusion criteria: Inability to consent to the study, ASA status >=3, coagulopathy, allergy to LA, prior surgery in the lumbosacral spine, body mass index >35 m/kg2, presence of pregnancy-related comorbidity (eg, gestational hypertension), gestational age 42 weeks, known fetal anomalies, active labor with cervical dilation >= 5 cm and increased risk of cesarean delivery (eg, vaginal birth after cesarean delivery).

Design outcomes

Primary

MeasureTime frame
percentage of patient with VAS=1 in 30 min after initial does;Onset time;

Secondary

MeasureTime frame
demographic date;VAS;Sensory blockade;modified Bromage score;Pruritus and nausea;Hypotension;Asymmetric blockade;Inadequate Analgesia;the time taken for epidural placement,;complications associated with epidural catheter;patient satisfaction;

Countries

China

Contacts

Public ContactLin Wenqian

The First Affiliated Hospital of Fujian Medical University

fymzk@outlook.com+86 18965086552

Outcome results

None listed

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