A clinical study on the prevention of postpartum urinary retention in analgesic delivery based on a new nursing intervention model based on MDT

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2500109848

Enrollment

Unknown

Registered

2025-09-25

Start date

2025-10-09

Completion date

Unknown

Last updated

2025-09-29

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

Conditions

Postpartum Urinary Retention

Interventions

experimental group:New Nursing Intervention Model for MDT

control group:Conventional nursing intervention model

Eligibility

Sex/Gender

Female

Age

20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Full-term pregnancy, aged 20 to 40 years old, receiving analgesic labor, and having signed the informed consent form.

Exclusion criteria

Exclusion criteria: Neurological disorders, organic lesions of the urinary system, history of skin allergies, etc.

Design outcomes

Primary

Measure	Time frame
incidence of urinary retention;	—

Secondary

Measure	Time frame
Negative emotions;Length of hospital stay;	—

Countries

China

Contacts

Public ContactWu Dan

The Second People's Hospital of Shenzhen

691160492@qq.com+86 137 1459 6581

Outcome results

None listed

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