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A single-center, prospective cohort study of an MR-based preoperative scoring system for predicting surgical capsular adhesions during prostatectomy

A single-center, prospective cohort study of an MR-based preoperative scoring system for predicting surgical capsular adhesions during prostatectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100049687
Enrollment
Unknown
Registered
2021-08-08
Start date
2021-09-30
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

Benign Prostatic Hyperplasia

Interventions

case series:N/A

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >= 50 years (when signing the informed consent form); 2. Clinical diagnosis of benign prostatic hyperplasia; 3. According to the actual needs of clinical diagnosis and treatment, the urologist will evaluate and plan laser enucleation of the prostate; 4. Provide the clinical data required for the research before surgery, and be willing to use the clinical information for further scientific research.

Exclusion criteria

Exclusion criteria: 1. At the same time combined with other pelvic malignancies (or have received pelvic floor surgery, radiotherapy); 2. Patients who do not want to participate in this observational study.

Design outcomes

Primary

MeasureTime frame
intraoperative surgical capsule adhesions;

Secondary

MeasureTime frame
the operation time of the prostate laser enucleation surgery;the operation time of comminution of the hyperplastic prostate tissue in bladder cavity;

Countries

China

Contacts

Public ContactMeng Yisen

Peking University First Hospital

mgyss@qq.com+86 10 83572481

Outcome results

None listed

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