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Effects of epidural analgesia and combined spinal-epidural analgesia on pelvic floor function of primiparous women

Effects of epidural analgesia and combined spinal-epidural analgesia on pelvic floor function of primiparous women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054382
Enrollment
Unknown
Registered
2021-12-16
Start date
2021-12-17
Completion date
Unknown
Last updated
2022-11-20

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

Conditions

pelvic floor function of primiparous women

Interventions

Experimental group1:Combined lumbar and epidural analgesia
Experimental group:Epidural labor pain relief

Sponsors

Jinan Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Suitable for primipara in vaginal delivery; 2. Aged 20 to 35 years; 3. Gestational age >= 37 weeks and < 42 weeks; 4. ASA classification II-III; 5. Single fetal head position; 6. The estimated fetal weight is greater than or equal to 2500 grams and less than 4000 grams; 7. Voluntary pelvic floor examination 42 days postpartum; 8. Obtain informed consent.

Exclusion criteria

Exclusion criteria: 1. History of urinary incontinence or fecal incontinence, pelvic organ prolapse, and pelvic surgery before pregnancy; 2. Pre-pregnancy body mass index > 25 kg/m2; 3. Heavy manual workers; 4. Long-term increased abdominal pressure (long-term cough > 1 month, long-term constipation); 5. There are contraindications for intraspinal labor analgesia.

Design outcomes

Primary

MeasureTime frame
Electrophysiological indexes of pelvic floor 42 days postpartum;Stress urinary incontinence symptoms at pregnancy and at 42 days after delivery of primipara;The maternal and neonatal outcomes at 42 days after delivery of primipara;

Countries

China

Contacts

Public ContactPang Yunting

Jinan Maternal and Child Health Hospital

pangyunting1209@126.com+86 18053156998

Outcome results

None listed

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