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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06037226
Other study ID # PekingUMCH-2021YFC20701303
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date September 2023
Est. completion date December 2024

Study information

Verified date October 2022
Source Peking Union Medical College Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In this protocol, our team intend to conduct a nation-wide multicenter cohort research to screening for PFD symptoms in early postnatal women in China. Beside clinically significant symptoms, we will also measure the recovery trend of pelvic muscle function, aiming to determine the clinically significant alterations that are sensitive to predict the PFD risks. This is an observational prospective cohort study, following a natural regular clinical visit process. Patients will voluntarily decide whether to receive PFD related treatments and the types of treatments to adopt. Therefore, we will also be able to compare the effectiveness of treatments.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 10000
Est. completion date December 2024
Est. primary completion date February 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria: 1. Postpartum women: 42 days+15 days after delivery 2. Age:20-45 3. Consent to participate in the research. Exclusion Criteria: 1. Refuse gynecological and/or obstetrical examinations. 2. Diagnosed with psychiatric disorders 3. Diagnosed with other severe illnesses 4. Received pelvic floor treatments 5. Other factors that may confound with the research

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Postpartum pelvic floor rehabilitation
biofeedback with Pelvic floor muscle training (PFMT)

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Peking Union Medical College Hospital

Outcome

Type Measure Description Time frame Safety issue
Other Pelvic muscle function In palpation, pelvic floor muscle strength will be graded based on the Oxford Muscle Scale and Electronic-muscle strength Medical Record system 6 months
Primary Urinary incontinence UI will be diagnosed via gynecological examination and self-reported symptoms 6 months
Secondary Pelvic organ prolapse Physical examinations will be performed to diagnose the incidence and degree of organ prolapse (i.e. anterior vaginal wall prolapse, posterior vaginal wall prolapse, uterine prolapse, and vaginal apex prolapse) according to the Pelvic Organ Prolapse Quantification (POP-Q). 6 months
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