NCT06282731

Brief Summary

The Changes of Urine Growth Factors Level in Patients With Benigh Prostate Hyperplasia after medical treatment.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
74

participants targeted

Target at P75+ for early_phase_1

Timeline
Completed

Started May 2013

Longer than P75 for early_phase_1

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 31, 2013

Completed
3.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2016

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 27, 2017

Completed
1.8 years until next milestone

First Submitted

Initial submission to the registry

February 11, 2019

Completed
5 years until next milestone

First Posted

Study publicly available on registry

February 28, 2024

Completed
Last Updated

February 28, 2024

Status Verified

February 1, 2024

Enrollment Period

3.3 years

First QC Date

February 11, 2019

Last Update Submit

February 21, 2024

Conditions

Keywords

Benigh Prostate Hyperplasia(BPH)Urine Growth Factors

Outcome Measures

Primary Outcomes (1)

  • Urine growth factors level

    Check Urine growth factors level after one month

    One month after medical treatment

Secondary Outcomes (1)

  • Urine growth factors level

    Three months after medical treatment

Other Outcomes (1)

  • Urine growth factors level

    Six months after medical treatment

Study Arms (1)

urine growth factor

OTHER

Previous studies have showed that overactive bladder syndrome (urge, frequency, nocturia or urinary incontinence) has been considered as an important factor to predict successful treatment. Urine nerve growth factor level, brain-derived neurotrophic factor and endothelium vascular growth factor have been proved as a simple and noninvasive biomarker for diagnosing overactive bladder.

Drug: Silodosin

Interventions

Indications:Benign prostate hyperplasia

Also known as: Tamsulosin HCl, Dutasteride, Doxazosin (methanesulfonate), Finasteride
urine growth factor

Eligibility Criteria

Age50 Years - 80 Years
Sexmale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • men with age 50\~80 years old
  • IPSS\>12
  • maximal flowrate 5\~15ml/sec
  • prostate size\>20ml
  • urine amount\>150ml
  • patient/family can sigh the inform concent

You may not qualify if:

  • prostate cancer or suspected prostate cancer(PSA\>4ng/ml)
  • history of prostate surgery
  • free of active urinary tract infection in past 6 months
  • patient with any other serious disease considered by investigator not in the condition to enter trials

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

En Chu Kong Hospital

New Taipei City, 23702, Taiwan

Location

Related Publications (51)

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MeSH Terms

Conditions

Prostatic Hyperplasia

Interventions

silodosinTamsulosinDutasterideDoxazosinmethanesulfonic acidFinasteride

Condition Hierarchy (Ancestors)

Prostatic DiseasesGenital Diseases, MaleGenital DiseasesUrogenital DiseasesMale Urogenital Diseases

Intervention Hierarchy (Ancestors)

BenzenesulfonamidesSulfonamidesAmidesOrganic ChemicalsBenzene DerivativesHydrocarbons, AromaticHydrocarbons, CyclicHydrocarbonsSulfonesSulfur CompoundsAzasteroidsSteroids, HeterocyclicSteroidsFused-Ring CompoundsPolycyclic CompoundsPrazosinQuinazolinesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-RingHeterocyclic CompoundsAndrostenesAndrostanes

Study Officials

  • Cheng Cheng Wang, M.D Ph.D

    Department of urology,En Chu Nong Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
early phase 1
Allocation
NA
Masking
NONE
Purpose
SCREENING
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Chief of Department of Urology

Study Record Dates

First Submitted

February 11, 2019

First Posted

February 28, 2024

Study Start

May 31, 2013

Primary Completion

September 1, 2016

Study Completion

April 27, 2017

Last Updated

February 28, 2024

Record last verified: 2024-02

Data Sharing

IPD Sharing
Will not share

Locations