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Clinical Trials/NCT04342533
NCT04342533
Unknown
Not Applicable

Prospective Randomized Trial of Irritative Symptoms Severity Assessment After Holmium Laser Enucleation of the Prostate (HoLEP) Versus Thulium Fiber Laser Enucleation of the Prostate (ThuFLEP).

I.M. Sechenov First Moscow State Medical University1 site in 1 country140 target enrollmentApril 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
BPH
Sponsor
I.M. Sechenov First Moscow State Medical University
Enrollment
140
Locations
1
Primary Endpoint
severity of urinary incontinence
Last Updated
4 years ago

Overview

Brief Summary

The investigators hypothesize that the functional outcomes of both techniques are comparable. However, ThuFLEP might increase speed recovery of postoperative irritation and early stress urinary incontinence according to the Questionnaire for Urinary Incontinence Diagnosis (QUID) because of minimal tissue penetration depth of TFL.

Detailed Description

Thulium fiber laser enucleation of the prostate (ThuFLEP) has already shown the outcomes comparable to OSP with better safety profile (lower blood loss compared to OSP) and shorter hospital stay. TFL has the efficacy and safety proven in comparative trials, being a promising rival for HoLEP. The main features of TFL distinguishing it from Ho:YAG is its wavelength of 1.94 µm (leading to about three-fold increase in water absorption and lesser penetration depth of \<0.1 mm vs \>0.2 mm in Ho:YAG). With identical average and peak powers of 100 W, the laser does not burst tissues, allowing for clean and precise cutting instead. Conversely, Ho:YAG's average power is about 100 W and its presumable peak power is around 10-15 kW. With such an outburst of energy, each pulse of Ho:YAG creates a large vapor bubble which ruptures the tissue. This may be a possible reason for increased irritative symptoms in early postoperative period after HoLEP comparing to ThuFLEP. But all in all, the probable causes for such postoperative symptoms remain unclear so far, despite the fact that absence of irritation and incontinence is ought to be one quality marker of "Pentafecta". According to the idea of high-power impact, probably, decreasing of HoLEP power will mitigate these problems. On the one hand, low-power HoLEP is feasible, safe and effective modality for symptomatic BPO. However, the results remain controversial and there is lack of LP-HoLEP application data nowadays. May be, with another option, for instance OSP or monopolar enucleation, it is possible to solve the issues. But the discussion of the past years demonstrates that the presence of early SUI is not only a problem of EEP, but also underreported in other approaches in relieving BPO secondary to BPH.

Registry
clinicaltrials.gov
Start Date
April 1, 2020
End Date
October 10, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dmitry Enikeev, MD, PhD

Deputy director for research

I.M. Sechenov First Moscow State Medical University

Eligibility Criteria

Inclusion Criteria

  • LUTS presence, proven by:
  • IPSS questionnaire (Score \>20);
  • OR uroflowmetry result (Qmax \<10 ml/s);

Exclusion Criteria

  • Prostate volume \> 120 cc
  • Prostate cancer on pathology;
  • Urethral strictures;
  • Bladder calculi;
  • Prior prostate surgery;
  • Neurogenic bladder dysfunction.

Outcomes

Primary Outcomes

severity of urinary incontinence

Time Frame: change from 1 week to 6 months after surgery

Questionnaire for Urinary Incontinence Diagnosis (higher score means worse incontinence)

Secondary Outcomes

  • catheter stay(1 week after surgery)
  • functional outcomes(change from 3 to 6 months after surgery)
  • surgery duration(during surgery)
  • hemoglobin drop(1 day after surgery)
  • hospitalization length(1 week after surgery)
  • rate of intra- and perioperative adverse events(6 months follow up)

Study Sites (1)

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