Skip to content

Postpartum rehabilitation clinical verification research and application demonstration

Postpartum rehabilitation clinical verification research and application demonstration

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049916
Enrollment
Unknown
Registered
2021-08-10
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-04-19

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

Conditions

Postpartum uterus, breast, pelvic floor rehabilitation

Interventions

Intervention group:Ultrasound intervention
Control Group:Conventional treatment

Sponsors

West China Second Hospital of Sichuan Universit
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Full-term (gestational week ? 37 weeks) normal vaginal delivery or cesarean section for women; 2. Postpartum mothers who voluntarily breastfeed and have no contraindications to breastfeeding.

Exclusion criteria

Exclusion criteria: 1. Twins and multiple births, women with polyhydramnios; 2. No serious complications and complications; 3. Local skin ulceration of breast and lower abdomen; 4. Coagulation dysfunction with APTT time greater than 40s and platelet count less than 80x10^9/L; 5. Wear a pacemaker and install a cardiac stent.

Design outcomes

Primary

MeasureTime frame
Lochia end time;

Secondary

MeasureTime frame
Uterine contraction pain;Descent height of uterine fundus;Lactation onset time;lactation yield;VAS score for breast tenderness;Double milk induration softening rate;Depression scale assessment;appraisal of life quality;

Countries

China

Contacts

Public ContactNiu Xiaoyu

West China Second University Hospital, Sichuan University

hxfeynxy@163.com+86 18180609132

Outcome results

None listed

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