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Clinical validation and demonstration of postpartum rehabilitation

Clinical validation and demonstration of postpartum rehabilitation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052099
Enrollment
Unknown
Registered
2021-10-17
Start date
2021-11-01
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Postpartum pelvic floor dysfunction

Interventions

Ultrasound intervention observation group:Low intensity focused ultrasound therapy
Ultrasound intervention control group:No
Biofeedback electrical stimulation observation group:Kegel training and biofeedback electrical stimulation
Biofeedback electrical stimulation control group:Kegel training

Sponsors

West China Second Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Full-term (gestational week >= 37 weeks) normal vaginal delivery or cesarean section; 2. Postpartum voluntary lactation and no lactation contraindications.

Exclusion criteria

Exclusion criteria: 1. Twin and multiple parturient, polyamniotic fluid parturient; 2. No serious complications or complications; 3. Local skin ulceration of the breast and lower abdomen; 4. The APTT time of coagulopathy was more than 40s, platelet count was less than 80 x 10^9/L; 5. Wear cardiac pacemaker and install cardiac stent.

Design outcomes

Primary

MeasureTime frame
Uterine instauration;Degree of organ prolapse;Lochia termination time;Vaginal dynamic pressure;

Secondary

MeasureTime frame
Fundal descent height;Uterine contraction pain;

Countries

China

Contacts

Public ContactZhang Miao

Affiliated Hospital of North Sichuan Medical College

767941485@qq.com+86 13696001275

Outcome results

None listed

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