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Clinical Trials/NCT03157726
NCT03157726UnknownNot Applicable

Transurethral Plasmakinetic Enucleation of Prostate Versus Transurethral Resection of Prostate: A Multi-center Randomized Control Trial

Zhujiang Hospital1 site in 1 country294 target enrollmentStarted: October 11, 2017Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
294
Locations
1
Primary Endpoint
Qmax(Maximum urinary flow rate)

Study Overview

Brief 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.

Detailed Description

Benign prostatic hyperplasia (BPH) is the most common disease of middle aged and elderly people which cause urinary tract symptoms (LUTS). transurethral resection of prostate(TURP) , began to replace the traditional open surgery in 1930s, still is as the "gold standard" operation for surgical treatment of BPH. However, compared with the traditional open operation, TURP has the following flaws:(1), due to the incomplete resection , maximum flow rate(Qmax) after TURP is lower than Qmax after open surgery. (2), there are serious complications, such as water intoxication and hemorrhage. (3) TURP has limitation to large prostate.

Transurethral plasmakinetic enucleation of prostate(TUKEP), an operation mode devised by Liu Chunxiao Team in southern medical university urology department, have offset the advantage of TURP. 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. One the one hand, TUKEP effectively solve the situation that It should repeatedly cut and stop bleeding and difficultly find the surgical capsule in TURP, which obviously reduce the rate of bleeding, prostatic capsula perforation, transurethral resection syndrome(TURS) and External sphincter injury. On the other hand, TUKEP is the minimally invasive surgery. It also achieves the effect of open surgery resolving the residual gland and reoperation post TURP.

The investigators plan to setup a a multicentric randomized control trial with 4-year follow-up comparing perioperative and postoperative outcomes for TUKEP and TURP. Through analyzing the perioperative and postoperative data between TUKEP group and TURP group, The purpose demonstrating superiority of safety, efficacy and economic benefit in TUKEP group.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Care Provider, Outcomes Assessor)

Eligibility Criteria

Ages
50 Years to 80 Years (Adult, Older Adult)
Sex
Male
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Diagnose as BPH
  • Between 50 and 80 year-old
  • Prostate volume less than 120g
  • Meet any conditions (1). International Prostate Symptom Score (IPSS),≥12 quality of life score (QOL) ≥4 分 (2).Maximum urinary flow rate (Qmax) 15 ml/s or less (urine flow more than 150 ml) (3).Medication is not efficient (4).Repeated urinary retention (extubation failure more than one) (5).Schafer≥grade 2
  • The American association of anesthesia score (ASA) class 1 to 3
  • Sign the informed consent voluntarily and will be willing to follow-up

Exclusion Criteria

  • Combined with central nervous system lesions (such as cerebrovascular accident, Parkinson, multiple sclerosis, cauda equina injury, spinal cord lesions, etc.) and neurogenic bladder;
  • The combination of advanced malignant tumor or chronic wasting disease;
  • Patients with severe cardiopulmonary disease or severe mental disorders;
  • Acute urinary tract infection, urethral stricture;
  • There is a history of prostate and bladder surgery;
  • Combined with severe coagulopathy;
  • Postoperative pathology confirmed prostate cancer;
  • Poor compliance, and can not be followed up.

Outcomes

Primary Outcomes

Qmax(Maximum urinary flow rate)

Time Frame: 4 years

Maximum urinary flow rate was measured at 1, 3, 6, 12, 24, 36 and 48-month postoperatively

IPSS (International Prostate Symptom Score )

Time Frame: 4 years

International Prostate Symptom Score was measured at 1, 3, 6, 12, 24, 36 and 48-month postoperatively

Secondary Outcomes

  • International Index Of Erectile Function (IIEF-5)(4 years)
  • Postoperative hospital stay(1 month)
  • QOL(Quality of Life)(4 years)
  • Indwelling catheter time(1 month)
  • Hospitalization expenses(1 month)
  • Residual urine volume(4 years)
  • Claviendindo classification(4 years)
  • Postoperative irrigation(1 month)
  • Retreatment rate(4 years)
  • Prostate volume(4 years)
  • Operation time(up to 24 hours)
  • Prostate-specific antigen(PSA)(4 years)
  • Decrease in Haemoglobin in 24 hours post-operation(1 month)

Investigators

Sponsor
Zhujiang Hospital
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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