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The individualized design of epidural administration for labor analgesia

The individualized design of epidural administration for labor analgesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031729
Enrollment
Unknown
Registered
2020-04-08
Start date
2020-07-01
Completion date
Unknown
Last updated
2020-04-13

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

Conditions

labor pain

Interventions

Individual analgesia group:Individualized analgesic regimens
Standardized analgesia group:Standardized analgesic regimen

Sponsors

Hubei Maternal and Child Healthcare Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
22 Years to 36 Years

Inclusion criteria

Inclusion criteria: Aged 22-36 years, weight 52-88kg, ASA I or II grade, gestation >= 36 weeks, the head of a single fetus of the first mother, cervical dilatation 1~3cm, obstetrician evaluation can be performed for vaginal delivery (pelvis, head pelvis evaluation), and requires epidural labor analgesia.

Exclusion criteria

Exclusion criteria: 1. Patients with severe pregnancy complications (placental abruption, placenta previa, gestational diabetes mellitus, preeclampsia); 2. Patients with contraindications to intraspinal anesthesia or who have recently received opioid therapy.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale;satisfaction evaluation;Total labor time;Apgar Score;

Secondary

MeasureTime frame
Stress response factor;

Countries

China

Contacts

Public ContactHeng Xu

Hubei Maternal and Child Healthcare Hospital

xuheng00@qq.com+86 15307188610

Outcome results

None listed

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