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A Randomized Controlled Study of Precise Anatomic Enucleation and Resection for Benign Prostatic Hyperplasia

A Randomized Controlled Study of Precise Anatomic Enucleation and Resection for Benign Prostatic Hyperplasia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000032510
Enrollment
Unknown
Registered
2020-04-30
Start date
2020-05-01
Completion date
Unknown
Last updated
2020-05-04

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

Conditions

Benign Prostatic Hyperplasia

Interventions

Precise Anatomic Enucleation:HoLEP

Sponsors

Shanghai Ninth People's Hospital, School of Medicine, Shanghai Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
50 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Sign informed consent; 2. Chinese male aged 50-100 (including 50 years old, 100 years old); 3. Meet the western medical diagnostic criteria for benign prostatic hyperplasia; 2) IPSS >= 12 points; 3) prostate volume> 25 cm3; 4) maximum urine flow rate (Qmax) <15 ml / s; 5) PSA <= 4ng / ml or clinical Exclude prostate cancer. 5) Alpha receptor blocker (one of naftopidil, terazosin, afurazosin, tamsulosin, tamsulosin) and 5a reductase inhibition after at least 6 months before surgery Combination (finasteride). 4. Preoperative examination results must be completed within 30 days before enrollment.

Exclusion criteria

Exclusion criteria: 1. Illnesses or conditions that affect patients' understanding, following and / or following the research process; 2. One of the following conditions was confirmed before surgery: 1) neurogenic bladder dysfunction; 2) history of lower urinary tract injury or previous prostate or urethral surgery; 3) known bladder tumor; 4) known urethral stricture or Bladder neck contracture; 5) Combined with other advanced malignancies; 3. Contraindications to other operations and anesthesia; 4. Other circumstances that the researcher considers inappropriate to participate in the study.

Design outcomes

Primary

MeasureTime frame
Qmax;IPSS;QoL;

Secondary

MeasureTime frame
Volume of postoperative flushing fluid;Complications;

Countries

China

Contacts

Public ContactZhong Wang

Shanghai Ninth People's Hospital, School of Medicine, Shanghai Jiaotong University

zhongwang2010@sina.com+86 13301980998

Outcome results

None listed

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