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NCT05987085 Clinical Trial

Medical Weight Loss on Pelvic Floor Dysfunction

Weight Loss Clinical Trial

— WLPFD  

Official title:
Effect of Medical Weight Loss on Pelvic Floor Dysfunction: a Prospective Observational Study

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05987085
Other study ID # WLPFD-PUMCH
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 3, 2023
Est. completion date December 2024

Study information
Verified date August 2023
Source Peking Union Medical College Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this observational study is to learn about the effect of medical weight loss on the symptom of pelvic floor dysfunction in obese and overweight women. The main question it aims to answer is: whether medical weight loss improves symptoms of pelvic floor dysfunctions in obese or overweight women.

Recruitment information / eligibility
Status Recruiting
Enrollment 200
Est. completion date December 2024
Est. primary completion date December 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age 18 or higher - BMI 24 kg/m2 or higher - Willing to follow the weight loss plan set by the physician follow-up and complete this study Exclusion Criteria: - Urinary tract infection or gynecologic reproductive system infection in the past month - Treatment history of pelvic floor disorders - Pregnancy or delivery in the past half year - Women with severe systemic disease - No follow-up conditions

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Diet and exercise
Routine intervention included diet control and exercise

Locations
Country Name City State
China Peking Union Medical College Hospital Beijing Beijing

Sponsors (1)
Lead Sponsor Collaborator
Peking Union Medical College Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pelvic floor symptoms before and after medical weight loss At least half a year
Secondary To explore the related factors of symptom improvement in pelvic floor dysfunction At least half a year
Secondary To explore the improvement of quality of life before and after medical weight loss At least half a year
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