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Transurethral Plasmakinetic Enucleation of Prostate Versus Transurethral Resection of Prostate (ERP)

Primary Purpose

Benign Prostatic Hyperplasia

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Transurethral plasmakinetic enucleation of prostate
transurethral resection of prostate
Sponsored by
Zhujiang Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Benign Prostatic Hyperplasia focused on measuring benign prostatic hyperplasia, multicenter randomized control clinical trial, transurethral plasmakinetic enucleation of prostate, transurethral resection of prostate

Eligibility Criteria

50 Years - 80 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Diagnose as BPH
  2. Between 50 and 80 year-old
  3. Prostate volume less than 120g
  4. 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
  5. The American association of anesthesia score (ASA) class 1 to 3
  6. Sign the informed consent voluntarily and will be willing to follow-up

Exclusion Criteria:

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

Sites / Locations

  • Zhujiang Hospital of Southern Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

TUKEP(enucleation of prostate)

TURP(resection of prostate)

Arm Description

Patients accept TUKEP (transurethral plasmakinetic enucleation of prostate). The TUKEP procedure requires the use of a resectoscope, camera system and irrigation fluid. The system consists of a generator unit and a wire loop with an electrical current running, the beak of resectoscope was used to enucleation of prostate and the bipolar loop was used to cutting and coagulation, There are many manufacturers of Bipolar TURP systems. Any bipolar plasmakinetic system approved by the CFDA (Chinese food and drug administration) may be used for the study. The bipolar plasmakinetic system was set at 160 W for cutting and 100 W for coagulation.

Patients accept TURP (transurethral resection of prostate). The TURP procedure requires the use of a resectoscope, camera system and irrigation fluid. The system consists of a generator unit and a wire loop with an electrical current running through the loop used to cut prostate tissue and cauterize. Prostate tissue is cut away in small pieces and removed at the end of the procedure using irrigation. There are many manufacturers of TURP systems. Any monopolar and bipolar loop system approved by the CFDA (Chinese food and drug administration) may be used for the study. The bipolar plasmakinetic system was set at 160 W for cutting and 100 W for coagulation.

Outcomes

Primary Outcome Measures

Qmax(Maximum urinary flow rate)
Maximum urinary flow rate was measured at 1, 3, 6, 12, 24, 36 and 48-month postoperatively
IPSS (International Prostate Symptom Score )
International Prostate Symptom Score was measured at 1, 3, 6, 12, 24, 36 and 48-month postoperatively

Secondary Outcome Measures

QOL(Quality of Life)
The Quality of Life Score was measured at 1, 3, 6, 12, 24, 36 and 48-month postoperatively
International Index Of Erectile Function (IIEF-5)
International Index Of Erectile Function is a patient reporting outcomes measuring the erectile function at the baseline, 1,3,6,12, 24,36 and 48-month follow-up visits postoperatively.
Operation time
operation time
Postoperative hospital stay
Postoperative hospital stay
Indwelling catheter time
The time of indwelling catheter post-operation
Postoperative irrigation
The time of Postoperative irrigation
Decrease in Haemoglobin in 24 hours post-operation
Compared with the baseline, to demonstrate the blood loss during operation
Retreatment rate
The ratio of patient who need reoperation to remove urinary tract obstruction
Prostate-specific antigen(PSA)
To compare the Prostate-specific antigen between TUKEP and TURP at baseline, 1,3,6,12, 24,36 and 48-month follow-up visits.
Hospitalization expenses
Total costs for BPH treatment during Hospitalization. The cost of other diseases should be excluded
Prostate volume
Prostate volume is measured by ultrasound or MRI at the baseline, 1,3,6,12, 24,36 and 48-month follow-up visits
Residual urine volume
Residual urine in the bladder after urination(via abdominal ultrasonography) is measure at the baseline, 1,3,6,12, 24,36 and 48-month follow-up visits
Claviendindo classification
It is a grade for evaluating surgical complications at 1,3,6,12, 24,36 and 48-month follow-up visits

Full Information

First Posted
May 11, 2017
Last Updated
March 1, 2020
Sponsor
Zhujiang Hospital
Collaborators
Nanfang Hospital, Southern Medical University, The First Affiliated Hospital of Anhui Medical University, The First Affiliated Hospital of Nanchang University, Fourth Affiliated Hospital of Guangxi Medical University, First Affiliated Hospital of Fujian Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT03157726
Brief Title
Transurethral Plasmakinetic Enucleation of Prostate Versus Transurethral Resection of Prostate
Acronym
ERP
Official Title
Transurethral Plasmakinetic Enucleation of Prostate Versus Transurethral Resection of Prostate: A Multi-center Randomized Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
October 11, 2017 (Actual)
Primary Completion Date
June 6, 2020 (Anticipated)
Study Completion Date
June 1, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Zhujiang Hospital
Collaborators
Nanfang Hospital, Southern Medical University, The First Affiliated Hospital of Anhui Medical University, The First Affiliated Hospital of Nanchang University, Fourth Affiliated Hospital of Guangxi Medical University, First Affiliated Hospital of Fujian Medical University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Benign Prostatic Hyperplasia
Keywords
benign prostatic hyperplasia, multicenter randomized control clinical trial, transurethral plasmakinetic enucleation of prostate, transurethral resection of prostate

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
294 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
TUKEP(enucleation of prostate)
Arm Type
Active Comparator
Arm Description
Patients accept TUKEP (transurethral plasmakinetic enucleation of prostate). The TUKEP procedure requires the use of a resectoscope, camera system and irrigation fluid. The system consists of a generator unit and a wire loop with an electrical current running, the beak of resectoscope was used to enucleation of prostate and the bipolar loop was used to cutting and coagulation, There are many manufacturers of Bipolar TURP systems. Any bipolar plasmakinetic system approved by the CFDA (Chinese food and drug administration) may be used for the study. The bipolar plasmakinetic system was set at 160 W for cutting and 100 W for coagulation.
Arm Title
TURP(resection of prostate)
Arm Type
Active Comparator
Arm Description
Patients accept TURP (transurethral resection of prostate). The TURP procedure requires the use of a resectoscope, camera system and irrigation fluid. The system consists of a generator unit and a wire loop with an electrical current running through the loop used to cut prostate tissue and cauterize. Prostate tissue is cut away in small pieces and removed at the end of the procedure using irrigation. There are many manufacturers of TURP systems. Any monopolar and bipolar loop system approved by the CFDA (Chinese food and drug administration) may be used for the study. The bipolar plasmakinetic system was set at 160 W for cutting and 100 W for coagulation.
Intervention Type
Procedure
Intervention Name(s)
Transurethral plasmakinetic enucleation of prostate
Other Intervention Name(s)
TUKEP
Intervention Description
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.
Intervention Type
Procedure
Intervention Name(s)
transurethral resection of prostate
Other Intervention Name(s)
TURP
Intervention Description
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.
Primary Outcome Measure Information:
Title
Qmax(Maximum urinary flow rate)
Description
Maximum urinary flow rate was measured at 1, 3, 6, 12, 24, 36 and 48-month postoperatively
Time Frame
4 years
Title
IPSS (International Prostate Symptom Score )
Description
International Prostate Symptom Score was measured at 1, 3, 6, 12, 24, 36 and 48-month postoperatively
Time Frame
4 years
Secondary Outcome Measure Information:
Title
QOL(Quality of Life)
Description
The Quality of Life Score was measured at 1, 3, 6, 12, 24, 36 and 48-month postoperatively
Time Frame
4 years
Title
International Index Of Erectile Function (IIEF-5)
Description
International Index Of Erectile Function is a patient reporting outcomes measuring the erectile function at the baseline, 1,3,6,12, 24,36 and 48-month follow-up visits postoperatively.
Time Frame
4 years
Title
Operation time
Description
operation time
Time Frame
up to 24 hours
Title
Postoperative hospital stay
Description
Postoperative hospital stay
Time Frame
1 month
Title
Indwelling catheter time
Description
The time of indwelling catheter post-operation
Time Frame
1 month
Title
Postoperative irrigation
Description
The time of Postoperative irrigation
Time Frame
1 month
Title
Decrease in Haemoglobin in 24 hours post-operation
Description
Compared with the baseline, to demonstrate the blood loss during operation
Time Frame
1 month
Title
Retreatment rate
Description
The ratio of patient who need reoperation to remove urinary tract obstruction
Time Frame
4 years
Title
Prostate-specific antigen(PSA)
Description
To compare the Prostate-specific antigen between TUKEP and TURP at baseline, 1,3,6,12, 24,36 and 48-month follow-up visits.
Time Frame
4 years
Title
Hospitalization expenses
Description
Total costs for BPH treatment during Hospitalization. The cost of other diseases should be excluded
Time Frame
1 month
Title
Prostate volume
Description
Prostate volume is measured by ultrasound or MRI at the baseline, 1,3,6,12, 24,36 and 48-month follow-up visits
Time Frame
4 years
Title
Residual urine volume
Description
Residual urine in the bladder after urination(via abdominal ultrasonography) is measure at the baseline, 1,3,6,12, 24,36 and 48-month follow-up visits
Time Frame
4 years
Title
Claviendindo classification
Description
It is a grade for evaluating surgical complications at 1,3,6,12, 24,36 and 48-month follow-up visits
Time Frame
4 years

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shaobo Zheng, M.D
Phone
13602888356
Email
1h1h1h864@sina.com
First Name & Middle Initial & Last Name or Official Title & Degree
ChunXiao Liu, M.D., Ph.D
Phone
13302296795
Email
liuchx888@hotmail.com
Facility Information:
Facility Name
Zhujiang Hospital of Southern Medical University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510282
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shaobo SB Zheng, M.D
Phone
+86-13602888356
Email
1h1h1h864@sina.com
First Name & Middle Initial & Last Name & Degree
ChunXiao CX Liu, M.D., Ph.D
Phone
+86-13302296795
Email
liuchx888@hotmail.com

12. IPD Sharing Statement

Plan to Share IPD
No

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Transurethral Plasmakinetic Enucleation of Prostate Versus Transurethral Resection of Prostate

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