Pelvic organ prolapse
Conditions
Interventions
Control group:Routine clinical assessment only. Medical records, imaging data, and gynecological examination findings are provided, and the surgical procedure is determined by two experienced gynecolo
Trial group:In addition to routine clinical data, a three-dimensional visualization model of the uterosacral ligament is used, and the surgical procedure is determined by two experienced gynecologists
Sponsors
Zhengzhou Central Hospital Affiliated to Zhengzhou University
Eligibility
Sex/Gender
Female
Age
36 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Women seeking surgical treatment primarily for pelvic organ prolapse; 2. Aged >= 30 years and <= 60 years; 3. POP-Q stage II-IV before surgery.
Exclusion criteria
Exclusion criteria: 1. Previous pelvic surgery for urinary incontinence, pelvic organ prolapse, or other pelvic floor dysfunction; 2. Previous pelvic surgery, radiotherapy, or chemotherapy for benign or malignant gynecological diseases; 3. Severe systemic diseases, such as unstable diabetes, heart disease, or malignant tumors in other body sites; 4. Contraindications to MRI, such as an intrauterine device, hip joint metallic implants, or a cardiac pacemaker.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Surgical protocol compliance rate;Length of uterosacral ligament;Volume of uterosacral ligament;Curvature of uterosacral ligament;Angle of uterosacral ligament;Pelvic organ prolapse quantification (POP-Q) stage; | — |
Countries
China
Contacts
Public ContactLi Xiaoge
Zhengzhou Central Hospital Affiliated to Zhengzhou University
Outcome results
None listed