Urinary Urinary Nerve Growth Factor (NGF) as a Biomarker for Mixed Urinary Incontinence

NCT ID: NCT01493401

Last Updated: 2019-12-02

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 137 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-02-28
• Study Completion Date: 2016-01-31

Brief Summary

Female urinary incontinence (UI) can be caused by pure stress UI (SUI), pure urgency UI (UUI) and mixed SUI and UUI (MUI). Clinically it might not be that easy to separate MUI and SUI. Patients might perceive urgency when they have an incompetent urethra and a full bladder.

Urinary tract nerve growth factor (NGF)is produced by bladder urothelium and smooth muscle. Increased levels of NGF have been reported in the bladder tissue and urine of patients with overactive bladder (OAB).

If the urinary levels of NGF differ among women with pure SUI and MUI, then urinary NGF level might be a biomarker in the differential diagnosis of MUI in women.

Also, decreased urinary NGF level was reported in OAB patients of whom the symptoms were improved. So, we might expect that the remnant OAB symptom including urgency incontinence can be improved, if the urinary NGF levels decrease after midurethral slings for SUI in MUI patients.

We aimed to explore the value of the urinary NGF as a biomarker for differential diagnosis and as a prognostic marker for predicting the improvement of OAB symptom after midurethral slings.

Conditions

Mixed Urinary Incontinence

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Midurethral sling

Currently available midurethral procedures for stress urinary incontinence can be used.

Group Type: EXPERIMENTAL

Midurethral slings (MUS)

Intervention Type: PROCEDURE

Retropubic, Transobturator, and Single incision MUS can be used.

Interventions

Midurethral slings (MUS)

Retropubic, Transobturator, and Single incision MUS can be used.

Intervention Type: PROCEDURE

Other Intervention Names

TVT, TVT-O, TOT, TVT-Secur, Needleless, etc.

Eligibility Criteria

Inclusion Criteria

• Women aged 18 or over 18 years with MUI for 3 or over 3 months
• Proven SUI by urodynamic study (UDS)or stress test
• Abdominal leak point pressure (ALPP)of 120 or less than 120cmH2O in UDS
• Symptoms verified using 5 day bladder diary as below i) number of urgency incontinence; 3 or more than 3/5days ii) number of micturition; 8 or more than 8/24hrs iii) number of urgency; 2 or more than 2/24hrs
• Women who cannot be pregnant or do not have plan to be pregnant
• 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

• The subject has WBC≧3, Albumin≧+1, Nit ≧+1 upon urinalysis
• On an unstable dosage of any drug with anticholinergic side effects, or expected to start such treatment during the study
• Patient has a significant pelvic orgen prolapse (POP) of ICS Stage 3 or over 3.
• Patients with combined POP surgery.
• Patients with bladder outlet obstruction on UDS or physical exam
• Patients with detrusor underactivity
• Diagnosed or suspected interstitial cystitis or bladder cancer
• History of radiation therapy on pelvic cavity
• Patients with neurologic condition which can affect lower urinary tract function
• History of urogenical malignancy within recent 2 years
• Treatment within the 14 days preceding enrollment, or expected to initiate treatment during the study with:

i)Any anticholinergic drugs and any drug treatment affecting lower urinary tract function Estrogen treatment started more than 2 months prior to inclusion is allowed. ii) electrostimulation, bladder training, electromagnetic treatment

• Patient is on anti-coagulation therapy.
• Any other condition which, in the opinion of the investigator, makes the patient unsuitable for inclusion

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Samsung Medical Center

OTHER

Sponsor Role: lead

Responsible Party

KYU-SUNG LEE

Urology, Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Kyu-Sung Lee, Ph.D

Role: PRINCIPAL_INVESTIGATOR

Samsung Medical Center

Locations

The Catholic University of Korea College of Medicine, Bucheon St. Mary's Hospital

Bucheon-si, , South Korea

Samsung Medical Center, Sungkyunkwan University School of Medicine

Seoul, , South Korea

Countries

South Korea

Other Identifiers

2009-11-068

Identifier Type: -

Identifier Source: org_study_id