Prognostic Value of the Urinary Nerve Growth Factor in the Patients With Benign Prostatic Hyperplasia

Overactive Detrusor Clinical Trial

Official title:

Prognostic Value of the Urinary Nerve Growth Factor (NGF) in the Patients With Benign Prostatic Hyperplasia (BPH) Who Undergo Holmium Laser Enucleation of the Prostate (HoLEP)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01781117
• Other study ID #: 2012-11-013
• Status: Completed
• Phase: N/A
• Start date: February 2013
• Est. completion date: January 2017

Study information

• Verified date: November 2019
• Source: Samsung Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Persistent detrusor overactivity (DO) after transurethral prostatectomy results in symptomatic failure in more than one third of the patients. Storage symptoms are major complaints in the early postoperative period after Holmium Laser Enucleation of the Prostate (HoLEP). Levels of the urinary nerve growth factor (NGF), produced by bladder urothelium and smooth muscle, are increased in the patients with overactive bladder (OAB), and decreased after the OAB symptoms were improved. Also, urinary NGF levels are increased in patients with benign prostatic obstruction (BPO), but the changes of the NGF levels after relief of the BPO by the medical or surgical treatment have not been fully investigated. If the elevated urinary NGF levels are reduced after successful surgical treatment of BPO, measurement of urinary NGF could be a useful objective tool to assess the therapeutic outcomes of the operation.

The aims of this study are to measure the urinary NGF levels in patients with BPO and to compare the results between the patients with detrusor overactivity (DO) and without detrusor overactivity (Non-DO), average 2 weeks before Holmium Laser Enucleation of the Prostate (HoLEP) procedure. After HoLEP, urinary NGF levels are rechecked at the periods of postoperative 3 months and 6 months, and compare changes between the two groups.

Description:

• Investigators are going to enroll age-matched control group and measure the urinary NGF levels as a baseline value (30 males).

• Investigators are going to enroll BPO patients group (DO group 50 and Non-DO group 50 patients).

• Administration of the anti-cholinergic agents was reported to decrease urinary NGF levels. Investigators are going to try to avoid the effect of anti-muscarinic drugs.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 184
• Est. completion date: January 2017
• Est. primary completion date: November 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 50 Years to 80 Years

Eligibility

Inclusion Criteria:

• Male aged 50 yrs or greater

• International prostatic symptom score >= 12

• Bladder outlet obstruction confirmed by pressure-flow study (BOOI > 20)

• Ability and willingness to correctly complete the micturition diary and questionnaire

• Capable of understanding and having signed the informed consent form after full discussion of the research nature of the treatment and its risks and benefits

Exclusion Criteria:

• Patients with urologic malignancies such as prostate cancer and bladder cancer

• Patients underwent urethral, prostate surgery

• Patients with urethral stricture or bladder diverticulum or bladder neck contracture

• Any other condition which, in the opinion of the investigator, makes the patient unsuitable for inclusion

Related Conditions & MeSH terms

• Benign Prostatic Hypertrophy With Outflow Obstruction
• Hyperplasia
• Hypertrophy
• Overactive Detrusor
• Prostatic Hyperplasia
• Urinary Bladder, Overactive

Intervention

Procedure:
• Holmium Laser Enucleation of the Prostate (HoLEP)
Enucleation of the enlarged nodule of prostate and morcellation of the resected tissue.

Device:
• Holmium laser enucleation system and morcellator
Holmium laser enucleation and morcellation

Locations

Country	Name	City	State
Korea, Republic of	Samsung Medical Center	Seoul

Sponsors (2)

Lead Sponsor	Collaborator
KYU-SUNG LEE	Samsung Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Difference in the serum PSA (Prostate Specific Antigen) level between the patients with or without detrusor overactivity		6 months after HoLEP procedure
Primary	Difference in the baseline urinary NGF level between patients with and without detrusor overactivity at 6 months after HoLEP procedure		6 months after HoLEP procedure
Secondary	Difference in the IPSS (International Prostate Symptom Score) and uroflowmetry results between the patients with or without detrusor overactivity		6 months after HoLEP procedure