Transurethral Plasmakinetic Enucleation of Prostate Versus Transurethral Resection of Prostate
NCT03157726 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 294
Last updated 2020-03-03
Summary
The study is a multicentric randomized control trial with 4-year follow-up comparing perioperative and postoperative outcomes for transurethral plasmakinetic enucleation of prostate(TUKEP) and transurethral resection of prostate(TURP). The investigators recruit patient with benign prostatic hyperplasia(BPH) as the object of study. TURP is set as control group . Meanwhile TUKEP is set as test group. Six affiliated hospitals will participate in this study. Through analyzing the perioperative and postoperative data between TUKEP group and TURP group, The investigators purpose demonstrating superiority of safety, efficacy and economic benefit in TUKEP group.
Conditions
- Benign Prostatic Hyperplasia
Interventions
- PROCEDURE
-
Transurethral plasmakinetic enucleation of prostate
Transurethral plasmakinetic enucleation of prostate(PAKEP),an operation mode devised by Liu Chunxiao Team in southern medical university urology department. The theory of the operation is using transurethral resectoscope instead of the finger in the open operation, to find the surgical capsule of prostate and to peel the hyperplastic prostate gland visually in a antidromic way.
- PROCEDURE
-
transurethral resection of prostate
Transurethral resection of prostate(TURP), a kind of mature minimally invasive surgery of prostate , taking the place of the traditional open surgery in 1930s , still is the "gold standard" operation for surgical treatment of BPH.
Sponsors & Collaborators
-
Nanfang Hospital, Southern Medical University
collaborator OTHER -
The First Affiliated Hospital of Anhui Medical University
collaborator OTHER -
The First Affiliated Hospital of Nanchang University
collaborator OTHER -
Fourth Affiliated Hospital of Guangxi Medical University
collaborator OTHER -
First Affiliated Hospital of Fujian Medical University
collaborator OTHER -
Zhujiang Hospital
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 50 Years
- Max Age
- 80 Years
- Sex
- MALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-10-11
- Primary Completion
- 2020-06-06
- Completion
- 2021-06-01
Countries
- China
Study Locations
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