search
Back to results

Low Energy HoLEP on IPSS

Primary Purpose

Prostate Hyperplasia, Prostatic Hypertrophy, Surgery

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Holmium laser
Sponsored by
Seoul National University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Hyperplasia

Eligibility Criteria

50 Years - 90 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers
  • Selection criteria Men over 50 Patients receiving HoLEP due to an enlarged prostate Patients who fully understood and agreed to the study
  • Exclusion criteria Patients with neuropathy that may adversely affect the urination function (Parkinson's disease, dementia, etc.) Patients with acute urinary lung disease within the last month Patients with symptomatic urinary tract infection In case there are other factors that can significantly affect treatment results at the discretion of the researcher

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    low energy holmium laser

    high energy holmium laser

    Arm Description

    30 watts

    80-100 watts

    Outcomes

    Primary Outcome Measures

    IPSS total score
    International Prostate Symptom Score

    Secondary Outcome Measures

    surgery time, total energy, resected prostate volume, immediate complication
    surgery related outcomes
    IPSS-subscore, IPSS-QoL, OABSS total score
    International Prostate Symptom Score
    Qmax, post voided residual urine volume
    efficacy outcomes

    Full Information

    First Posted
    August 13, 2020
    Last Updated
    August 13, 2020
    Sponsor
    Seoul National University Hospital
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT04514718
    Brief Title
    Low Energy HoLEP on IPSS
    Official Title
    Short- and Medium-term Safety/Effectiveness Analysis of Low Energy Holmium Laser Enucleation of the Prostate (HoLEP)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2020
    Overall Recruitment Status
    Unknown status
    Study Start Date
    August 24, 2020 (Anticipated)
    Primary Completion Date
    December 31, 2020 (Anticipated)
    Study Completion Date
    December 31, 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Seoul National University Hospital

    4. Oversight

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

    5. Study Description

    Brief Summary
    The purpose of this study is to prove that low-energy (30W) Holmium laser prostatectomy (Holeb) is not inferior to high-energy (100W) Holmium laser prostatectomy (safety and effectiveness)
    Detailed Description
    Overview of the study Research design: prospective, single-arm blind randomized control study, non-inferiority study Study Period: 12 months since IRB approval date Subject: Patients with benign prostatic hyperplasia Number of study subjects: 90 Vulnerable Subjects: None Background and purpose of the study 1) Research background Overview and main symptoms of prostatic hyperplasia (BPH) -The prostate is a male reproductive organ located in the lower bladder. Benign prostatic hyperplasia (BPH) causes lower urinary tract symptoms (LUTS) due to bladder outlet obstruction. The prevalence of prostatic hyperplasia is known to reach 37% in the 50s, 49% in the 60s, and 70% in the 70s; a disease with a very high incidence in long-aged men. BPH is a disease directly related to the quality of life that interferes with the patient's social life, sexual life, and daily life. If it persists for a long time, it may cause bladder stones, hematuria, and even renal dysfunction, so timely treatment is absolutely necessary. Surgical Treatment of BPH -Surgical treatment is recommended for an enlarged prostate that is not treated with drugs, and transurethral surgery using an endoscope is recommended for standard surgery for an enlarged prostate. Transurethral surgery for BPH varies from traditional transurethral resection of the prostate (TURP) to holmium laser enucleation of the prostate (HoLEP). HoLEP has a sharp increase in the number of surgeries worldwide due to its low recurrence rate, high efficiency, and high patient satisfaction; Since its first introduction in 2008 in Korea, the number and rate of surgeries have been steadily increasing. The total number of surgery for BPH is equivalent to about 10,000 cases per year. TUR-P and KTP laser surgery are on a decreasing trend, while HoLEP is on an increasing trend. The importance of HoLEP -HoLEP is a surgery to completely remove prostate tumors using a Holmium-YAG Laser of 2100nm wavelength. -The tissue penetration depth of the Holmium laser is less than 0.44mm, enabling sharp incisions, and has the advantage of less bleeding than traditional transurethral prostatectomy. -The surgery principle of HoLEP is fundamentally different from TUR-P and KTP laser prostate vaporization. TUR-P and KTP laser prostatectomy aim to remove part of the prostate tumor, whereas HoLEP performs complete removal of the prostate tumor according to the anatomical structure. -HoLEP consists of two steps, and the first step consists of an enucleation step in which the prostate tumor is completely removed and placed in the bladder, and a morcellation step in which the enucleated adenoma tissue is morcellated and removed. HoLEP is relatively safe compared to other transurethral surgery and can completely remove prostate adenoma, so it has a low recurrence rate and the patient's satisfaction with surgery is over 90%, making it the next-generation standard treatment for BPH. Low energy HoLEP related research and clinical status -HoLEP is mainly applied to treatment with 80-100 Watt high energy equipment. High-energy HoLEP has the advantage of removing prostate tumors in a short time, but there are problems of frequent laser fiber damage, device shutdown problems, and possible bladder damage due to scattered lasers. In 2008, Rassweiller et al. proposed the possibility of clinical application of low energy HoLEP by applying a 40 Watt Holmium laser. Since then, prospective studies have been published sporadically. In 2018, a prospective randomized study that compared and analyzed the prostate removal efficiency of 50 Watt laser and 100 Watt laser in a total of 121 patients was the latest and largest study and confirmed that low-energy prostatectomy is not inferior to the high-energy procedure. And proved its clinical safety. In theory, low-energy HoLEP reduces dysuria immediately after surgery and storage symptoms after surgery. It is estimated to be advantageous in preserving erectile function. The research team is the first in the world to compare the safety and usefulness of 30 Watt HoLEP with 100 Watt HoLEP through prospective, non-inferiority studies. 2) Research goal The final purpose of the study: To prove that the low-energy (30Watt) HoLEP is not inferior to the high-energy (100Watt) HoLEP in short-term and mid-term surgical results (safety and effectiveness). Detailed research objectives: Compare short-term (2 weeks-1 months) surgical outcomes/surgical complications of low energy HoLEP with high energy HoLEP. Compare the mid-term (3, 6 months) surgical outcomes/surgical complications of low-energy HoLEP with high-energy HoLEP. 3) Selection criteria, exclusion criteria, the target number of subjects and basis for calculation Selection criteria Men over 50 Patients receiving HoLEP due to an enlarged prostate Patients who fully understood and agreed to the study Exclusion criteria Patients with neuropathy that may adversely affect the urination function (Parkinson's disease, dementia, etc.) Patients with acute urinary retention within the last month Patients with symptomatic urinary tract infection In case there are other factors that can significantly affect treatment results at the discretion of the researcher (2) Number of research subjects About 90 patients The basis for calculating the number of subjects This study aims to prospectively enroll and randomize prostatectomy patients, and then compare the results of the treatment at 6 months after the maximum operation to confirm non-inferiority. The current standard is a method using a high-energy holmium laser, and the treatment results for 6 months after surgery have been published through many studies. The research team wants to confirm the surgical outcome as a decrease in the International Prostate Symptom Score (IPSS). After 6 months of predicted high-energy HoLEP, IPSS in other literature (5.1 ± 5.0), 6 months after the expected of low-energy HoLEP. IPSS is estimated from the most recently published academic paper (5.0 ± 5.0). Alpha (0.15) and Beta (0.8) were calculated, and the non-inferior margin was set to 3. The estimated number of subjects is calculated by considering the 20% drop-out rate. Statistics for calculating the number of subjects are calculated using PASS 2019. Considering drop-out 20%, it is necessary to recruit 25-114 patients (total 50-114) per group to conduct the study. This organization is an organization that implements about 20-30 HoLEP cases per month, and a follow-up period of up to 6 months is required to announce short-term and mid-term results. Therefore, the actual patient enroll period is estimated to be up to 6 months. It is expected that 120-180 patients can undergo surgery during the recruitment period of up to 6 months, and assuming that only 60% of patients will participate in the study based on the median of about 150, a total of 90 patients, about 45 for each group. It is judged realistic to conduct a study with 3 patients. 4. Research method Specific research method Since the researchers have already published dozens of studies related to HoLEP surgery, we are securing a systematic preoperative examination/postoperative follow-up process. The preoperative examination/postoperative follow-up protocol of high energy HoLEP surgery, which was previously performed, will be used as it is, but the study will be conducted by adding only the preoperative randomization process. -Pre-screening: After making operation in the outpatient clinic, before hospitalization, it is checked whether it is subject to enroll according to the patient record. -Random allocation: Using R package (RandomizeR), low energy HoLEP, and high energy HoLEP is randomly assigned. -Pre-Op work-up & Operation: This item is irrelevant to Randomization and is a situation where you do not know who will undergo surgery, so it is considered a normal treatment process and proceeds according to the existing process. Monitoring: It is planned to perform research ethics, safety, and monitoring work independently from the researcher by requesting the Medical Device Innovation Center. Clinical trial insurance: In case of adverse side effects to patients, the company plans to subscribe to clinical trial liability insurance through the Medical Device Innovation Center to notify the patient of the procedures and details of the clinical trial damage relief. Compensation: There is no monetary incentive for research participants, and the research team will pay 30,000 won of transportation and inspection costs (160,000 won) per visit during the participation period of visit #1-#3. Test drug administration/dosage, administration/use method, combination therapy, reasons for selection when using a reference drug None Observation items, clinical test items and observation test methods Primary endpoint: 3-6 month questionnaire (International Prostate Symptom Score, IPSS) total score Secondary endpoint: 1) Surgery day: surgery time, total energy, resected prostate volume, immediate complication 1) 2 weeks after surgery: questionnaire (IPSS-subscore, IPSS-QoL, OABSS total score), Qmax, 2) post voided residual urine volume, Clavian-Dindo complication classification 3) 3, 6 months after surgery: questionnaire (IPSS-total, IPSS subscore, IPSS-QoL, OABSS total score), Qmax, post voided residual urine volume, Clavian-Dindo complication classification, urine test (urinalysis, urine microscopy), serum PSA level 4) Effect evaluation criteria, evaluation method Efficacy Statistical analysis of low-power HoLEP is not inferior in short-term (2wk/1month) and mid-term (3-6 months) IPSS. Uroflowmetry (UFM) and non-inferiority of post voided residual (PVR) were verified in urinalysis. 3 months/6 months U/A, micro, 6 months PSA Non-inferiority was verified in terms of improving the patient's QoL. To verify the non-inferiority of the storage symptom subscore after the patient's surgery. Safety: The safety of HoLEP has been revealed to some extent through overseas research results, so animal testing is not required. For the safety, all safety issues that occurred using the Clavian-Dindo grade, which are commonly used clinically in human studies, were recorded and compared and analyzed. If adverse events that occurred immediately after surgery and during up to 3 visits were recorded and there was a statistically significant difference in complications of Grade III-IV, it was judged that there was a safety problem. 4) The difference between existing treatment and research Existing studies comparing low energy HoLEP surgery and high energy HoLEP are mostly retrospective studies, and two prospective studies have been performed. One of the two prospective studies involved 54 patients and had no active control group. The most recent study was RCT with 121 subjects, but it was a study comparing 50W laser and 100W laser. This study is the first in the world to compare 30W laser and 100W laser, and it is a prospective, RCT that recruits 90 patients, and it is judged that the results of the study can provide important medical evidence for the safety and effectiveness of low-energy HoLEP surgery.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Prostate Hyperplasia, Prostatic Hypertrophy, Surgery, Bladder Outlet Obstruction, Quality of Life, Complication of Surgical Procedure

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Allocation
    Randomized
    Enrollment
    90 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    low energy holmium laser
    Arm Type
    Active Comparator
    Arm Description
    30 watts
    Arm Title
    high energy holmium laser
    Arm Type
    Active Comparator
    Arm Description
    80-100 watts
    Intervention Type
    Device
    Intervention Name(s)
    Holmium laser
    Intervention Description
    low energy holmium laser
    Primary Outcome Measure Information:
    Title
    IPSS total score
    Description
    International Prostate Symptom Score
    Time Frame
    baseline, postoperative 3 months, and 6 months
    Secondary Outcome Measure Information:
    Title
    surgery time, total energy, resected prostate volume, immediate complication
    Description
    surgery related outcomes
    Time Frame
    Surgery day
    Title
    IPSS-subscore, IPSS-QoL, OABSS total score
    Description
    International Prostate Symptom Score
    Time Frame
    baseline, postoperative 3 months, and 6 months
    Title
    Qmax, post voided residual urine volume
    Description
    efficacy outcomes
    Time Frame
    baseline, postoperative 3 months, and 6 months

    10. Eligibility

    Sex
    Male
    Minimum Age & Unit of Time
    50 Years
    Maximum Age & Unit of Time
    90 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Selection criteria Men over 50 Patients receiving HoLEP due to an enlarged prostate Patients who fully understood and agreed to the study Exclusion criteria Patients with neuropathy that may adversely affect the urination function (Parkinson's disease, dementia, etc.) Patients with acute urinary lung disease within the last month Patients with symptomatic urinary tract infection In case there are other factors that can significantly affect treatment results at the discretion of the researcher

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Low Energy HoLEP on IPSS

    We'll reach out to this number within 24 hrs