FindTrial
Sign In

Postpartum uterine contraction pain after vaginal delivery: a prospective observational study

Postpartum uterine contraction pain after vaginal delivery: a prospective observational study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800014753
Enrollment
Unknown
Registered
2018-02-02
Start date
2018-03-01
Completion date
Unknown
Last updated
2018-02-05

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

Conditions

postpartum uterine contraction pain

Interventions

primiparas:labor analgesia
multiparas:labor analgesia

Sponsors

Shanghai First Maternity and Infant Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: no obstetric contraindications, single fetus, ASA I~II, vaginal delivery

Exclusion criteria

Exclusion criteria: abnormal of the fetus or newborns, mental abnormality of the subjects, the subjects were unable to understand the content of the questionnaire

Design outcomes

Primary

MeasureTime frame
pain locations;postpartum uterine contraction pain;—

Secondary

MeasureTime frame
postpartum perineal pain;—

Countries

China

Contacts

Public ContactXin Fang
fangxin@51mch.com+86 18616616167

Outcome results

None listed

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