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Contractility: Cuff Versus Urodynamics Testing In Males With Voiding Lower Urinary Tract Symptoms (CONCUR)

Primary Purpose

Lower Urinary Tract Symptoms

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Penile cuff test
Sponsored by
Newcastle-upon-Tyne Hospitals NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Lower Urinary Tract Symptoms focused on measuring bladder, urinary tract, symptoms, contractility, urodynamics, penile cuff test

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Male aged 18 years old or over
  • Referred for video urodynamics within our department
  • Predominant voiding LUTS as assessed by IPSS at screening. [The total IPSS score is out of 35, with up to 15 points for storage symptoms and 20 for voiding symptoms. If voiding symptoms as a percentage of total score is higher than storage symptoms they will be included in the study].
  • Capacity to understand study procedures and give informed consent
  • At least 2 voided volumes on frequency volume chart (FVC) of 250 mL

Exclusion Criteria:

  • Female patients
  • Long term catheterisation
  • Predominant storage LUTS on IPSS at screening
  • Fewer than 2 voids on FVC > 250 mL
  • Known pre-existing neurological cause for symptoms
  • Active urinary tract infection (UTI)

Sites / Locations

  • Freeman Hospital, Newcastle upon Tyne Hospitals NHS Foundation TrustRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Pilot group: urodynamics and cuff test

Arm Description

Single-arm study with all participants undergoing cystometrogram, then cystometrogram with simultaneous penile cuff test, then penile cuff test alone

Outcomes

Primary Outcome Measures

Difference between invasive and non-invasive measurements
Comparison of the pressure required to interrupt urine flow (pcuff.int) and simultaneously measured isovolumetric bladder pressure (pves.isv).

Secondary Outcome Measures

Change in variance
Comparison of results from this pilot study with analysis of past cohort to see if variances within the two populations are different (F test)
Assessment of bladder contractility - BCI
Invasive assessment of contractility using the bladder contractility index (BCI). (it will also be analysed for correlation with pcuff.int)
Assessment of bladder contractility - Watt's Factor
Invasive assessment of contractility using Watt's Factor (it will also be analysed for correlation with pcuff.int)
Quality of Life Assessment - ICIQ-MLUTS
International Consultation on Incontinence Modular Questionnaire for male LUTS (ICIQ-MLUTS) will be completed by the participant. This is a modular symptom and quality of life questionnaire, in which the participant scores the frequency of a symptom from 0-4, and completes a 0-10 bother score (10 =worst) for each symptom. There are 20 questions in total. ( and analysed for correlation with outcome 6)
Quality of Life Assessment - IPSS
International prostate symptoms score (IPSS) will be completed by the participant. Total score range 0-35 - generated from the sum of 7 questions related to urinary symptoms - all scored from 0-5 on degree of frequency. It will also be analysed for correlation with outcome 5)
Accuracy of ultrasound residual urine volume
catheterized post void residual volume will be used as a gold standard to compare ultrasound residual measurements from two clinicians

Full Information

First Posted
June 27, 2018
Last Updated
September 14, 2018
Sponsor
Newcastle-upon-Tyne Hospitals NHS Trust
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1. Study Identification

Unique Protocol Identification Number
NCT03603015
Brief Title
Contractility: Cuff Versus Urodynamics Testing In Males With Voiding Lower Urinary Tract Symptoms
Acronym
CONCUR
Official Title
Contractility: Cuff Versus Urodynamics Testing In Males With Voiding Lower Urinary Tract Symptoms
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Unknown status
Study Start Date
August 28, 2018 (Actual)
Primary Completion Date
March 2019 (Anticipated)
Study Completion Date
March 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Newcastle-upon-Tyne Hospitals NHS Trust

4. Oversight

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

5. Study Description

Brief Summary
A number of men will experience bothersome urinary symptoms, which become more common as they age. A number of conditions can cause these symptoms, and general practitioners may refer men to their local hospital for further assessment and treatment. Symptoms can include poor flow of urine, the need to pass urine more frequently, or the sensation that the bladder is not completely emptying. This can be due to an enlargement of the prostate gland. These symptoms can also be caused when the bladder muscle is not able to contract (squeeze) as well as it previously has to empty the bladder. This is known as underactive bladder (UAB). It is important to distinguish between the two conditions as a cause for these symptoms, to prevent side effects from unnecessary medications or operations. Currently, men would need to undergo a bladder pressure test (urodynamics). This involves inserting a catheter via the penis into the bladder, through which the bladder is filled with fluid and pressure is measured. A separate second small tube is inserted into the rectum to measure the pressure in the abdomen. The pressure changes are observed as the bladder is filled, and then urine is passed around the catheter. A second technique for measuring bladder pressure is the use of a small inflatable cuff which is placed around the penis (penile cuff test). The bladder pressure can then be determined by inflating the cuff and interrupting the flow of urine. The bladder can be filled naturally before the test, which means a bladder catheter tube is not required. This study is designed to find out ways that the penile cuff test can be made more accurate. It will compare the cuff results to those obtained from a bladder pressure test, and will take x-ray pictures of the urinary tract during the test.
Detailed Description
The investigators intend to refine the procedural steps of the cuff test to improve the measurement and reduce variability with pves.isv, therefore giving a more reproducible test. By improving the penile cuff test, the investigators can then go on to assess how our non-invasive measurements correlate with urodynamically derived indices of contractility, and use data from this pilot to help construct methodology of future cuff research. The current hypotheses are that; 1) accuracy of the cuff interruption pressure (pcuff.int) can be improved by modification of penile cuff test factors, 2) the number of valid inflations obtained per patient will increase with the modifications, and 3) that this non-invasive measure of contractility will correlate with pre-existing invasive indices. The research protocol also gives the opportunity to explore correlation between commonly used symptom scores, and accuracy in the assessment of ultrasound residual urine volume measurement. The primary objectives are therefore: To modify procedural steps of the penile cuff test that may reduce the previously observed variability and perform a pilot study to assess a reduction in variance To identify behaviour of the urethra during penile cuff inflation, by performing x-ray screening during the penile cuff test, and assess whether this is another source of inaccuracy To test the basic assumption of the penile cuff test that the bladder neck remains open during flow interruption Secondary objectives of the study include the following: To compare non-invasive measurements from the penile cuff test against invasive indices of contractility To compare 2 different symptom scores for men with voiding lower urinary tract symptoms (LUTS) To assess accuracy and inter-observer variability of ultrasound residual measurement against a known volume.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lower Urinary Tract Symptoms
Keywords
bladder, urinary tract, symptoms, contractility, urodynamics, penile cuff test

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Single pilot group all receiving the same tests
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Pilot group: urodynamics and cuff test
Arm Type
Other
Arm Description
Single-arm study with all participants undergoing cystometrogram, then cystometrogram with simultaneous penile cuff test, then penile cuff test alone
Intervention Type
Diagnostic Test
Intervention Name(s)
Penile cuff test
Other Intervention Name(s)
Cystometrogram
Intervention Description
Comparison of invasive vs non-invasive urodynamics
Primary Outcome Measure Information:
Title
Difference between invasive and non-invasive measurements
Description
Comparison of the pressure required to interrupt urine flow (pcuff.int) and simultaneously measured isovolumetric bladder pressure (pves.isv).
Time Frame
During the procedure
Secondary Outcome Measure Information:
Title
Change in variance
Description
Comparison of results from this pilot study with analysis of past cohort to see if variances within the two populations are different (F test)
Time Frame
During the procedure
Title
Assessment of bladder contractility - BCI
Description
Invasive assessment of contractility using the bladder contractility index (BCI). (it will also be analysed for correlation with pcuff.int)
Time Frame
During the procedure
Title
Assessment of bladder contractility - Watt's Factor
Description
Invasive assessment of contractility using Watt's Factor (it will also be analysed for correlation with pcuff.int)
Time Frame
During the procedure
Title
Quality of Life Assessment - ICIQ-MLUTS
Description
International Consultation on Incontinence Modular Questionnaire for male LUTS (ICIQ-MLUTS) will be completed by the participant. This is a modular symptom and quality of life questionnaire, in which the participant scores the frequency of a symptom from 0-4, and completes a 0-10 bother score (10 =worst) for each symptom. There are 20 questions in total. ( and analysed for correlation with outcome 6)
Time Frame
During the procedure
Title
Quality of Life Assessment - IPSS
Description
International prostate symptoms score (IPSS) will be completed by the participant. Total score range 0-35 - generated from the sum of 7 questions related to urinary symptoms - all scored from 0-5 on degree of frequency. It will also be analysed for correlation with outcome 5)
Time Frame
During the procedure
Title
Accuracy of ultrasound residual urine volume
Description
catheterized post void residual volume will be used as a gold standard to compare ultrasound residual measurements from two clinicians
Time Frame
During the procedure

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male aged 18 years old or over Referred for video urodynamics within our department Predominant voiding LUTS as assessed by IPSS at screening. [The total IPSS score is out of 35, with up to 15 points for storage symptoms and 20 for voiding symptoms. If voiding symptoms as a percentage of total score is higher than storage symptoms they will be included in the study]. Capacity to understand study procedures and give informed consent At least 2 voided volumes on frequency volume chart (FVC) of 250 mL Exclusion Criteria: Female patients Long term catheterisation Predominant storage LUTS on IPSS at screening Fewer than 2 voids on FVC > 250 mL Known pre-existing neurological cause for symptoms Active urinary tract infection (UTI)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Helen C Morton, MBBS
Phone
0191 2139602
Email
Helen.Morton@nuth.nhs.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Alison Bray, PhD
Phone
0191 2823823
Email
ABray3@nhs.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Helen C Morton, MBBS
Organizational Affiliation
Newcastle upon Tyne Hospitals NHS Foundation Trust
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Chris K Harding, MBBChir, MD
Organizational Affiliation
Newcastle upon Tyne Hospitals NHS Foundation Trust
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Alison Bray, PhD
Organizational Affiliation
Newcastle upon Tyne Hospitals NHS Foundation Trust
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
James Blake, PhD
Organizational Affiliation
Newcastle upon Tyne Hospitals NHS Foundation Trust
Official's Role
Study Director
Facility Information:
Facility Name
Freeman Hospital, Newcastle upon Tyne Hospitals NHS Foundation Trust
City
Newcastle
State/Province
Tyne And Wear
ZIP/Postal Code
NE7 7DN
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Helen C Morton, MBBS
First Name & Middle Initial & Last Name & Degree
Nicola Brown
Phone
(+44) 0191 2137322
Email
Nicola.Brown@nuth.nhs.uk

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Contractility: Cuff Versus Urodynamics Testing In Males With Voiding Lower Urinary Tract Symptoms

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