Effect of clinical application of labor analgesia on mother and infant

Information-based management of labor analgesia and its clinical application's influence on mothers and infants

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2100044067

Enrollment

Unknown

Registered

2021-03-09

Start date

2021-04-01

Completion date

Unknown

Last updated

2021-07-21

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

Conditions

clinical application of labor analgesia

Interventions

Receiving epidural labor analgesia group:Nil

Non epidural labor analgesia group:Nil

Eligibility

Sex/Gender

Female

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: The expectant mothers within the time limit of the project study, with complete hospitalization data, agree to participate and sign a written informed consent form, have follow-up conditions, and have good compliance with follow-up and management.

Exclusion criteria

Exclusion criteria: Severe pregnancy complications and complications, various high-risk mothers that may affect the effects of clinical interventions, and children with congenital diseases that affect intellectual behavior, such as pubic symphysis separation, psychiatric and neurological diseases, congenital hypothyroidism, trisomy 21, etc.

Design outcomes

Primary

Measure	Time frame
EPDS score;Gesell;	—

Secondary

Measure	Time frame
ICI-Q-SF score;	—

Countries

China

Contacts

Public ContactFeng Jifeng

Maternity and Child Care of Guangxi Zhuang Autonomous Region

604282082@qq.com+86 13768112111

Outcome results

None listed

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