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The Effect of Catheter Valve Vs. Standard Catheter Removal in Outpatients

Primary Purpose

Urinary Retention

Status
Unknown status
Phase
Phase 2
Locations
United Kingdom
Study Type
Interventional
Intervention
Use of catheter valve before 'trial removal of catheter'
Trial removal of catheter in patients with urinary retention
Sponsored by
Medway NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urinary Retention focused on measuring Urinary retention, trial removal of catheter, valve

Eligibility Criteria

60 Years - 85 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Men aged 60-85 catheterised for urinary retention and booked for outpatient removal of catheter
  • Mobile patients

Exclusion Criteria:

  • Who cannot consent
  • Residual urine of more then 1 litre
  • Abnormal renal functions
  • Poor manual dexterity
  • Learning difficulties/dementia.

Sites / Locations

  • Medway NHS Foundation TrustRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Without valve

With valve

Arm Description

Trial removal of catheter without catheter valve in patients with urinary retention. These are those patients who have catheter on free drainage, attend the clinic for catheter removal and bladder to be filled naturally ( which may take upto 4-5 hours). After removal of catheter they will be asked to drink plenty of fluids while waiting for the bladder to fill up. This is the traditional method of catheter removal.

Trial removal of catheter in patients with urinary retention with closed catheter valve. These patients will be asked to close the valve 3-4 hours before attending the clinic prior to catheter removal. Here the intervention is catheter valve that allows bladder to be comfortably full by the time patient arrives in the clinic. By this intervention the investigators hypothesise that the investigators can save the clinic time as the patient will not need to wait for natural bladder filling which generally takes 4-5 hours. Intervention: Urinary catheter valve

Outcomes

Primary Outcome Measures

Time to spontaneous void after catheter removal
The primary outcome measure of this study is to see if usage of catheter valve results in early spontaneous voiding after catheter removal and thus significantly reduces the time spent by these patients in the clinic.

Secondary Outcome Measures

Complications associated with valve
To see if the patients with the catheter valve have more complications (catheter bypass, urinary tract infection and pain).
Reduction in clinic waiting time (hours)
To see if usage of catheter valve results in early discharge after catheter removal resulting in reduction of time spent in the clinic (in hours)
Reduction in the cost of running the clinic
To see if reduction in the time spent by the catheter valve patients results in reducing the cost of running of the TWOC (Trial without catheter) clinic (in British Pound Sterling).

Full Information

First Posted
January 20, 2016
Last Updated
March 25, 2016
Sponsor
Medway NHS Foundation Trust
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1. Study Identification

Unique Protocol Identification Number
NCT02717975
Brief Title
The Effect of Catheter Valve Vs. Standard Catheter Removal in Outpatients
Official Title
A Prospective, Multicenter, Randomized Trial: The Effect of Catheter Valve Vs. Standard Catheter Removal in Outpatient Settings on the Patient Discharge Timings
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Unknown status
Study Start Date
March 2016 (undefined)
Primary Completion Date
March 2017 (Anticipated)
Study Completion Date
May 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medway NHS Foundation Trust

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
It is estimated that over 10% of men above the age of 60 will experience an episode of urinary retention over a period of 5 years and will need urethral catheter. Some of these patients are discharged from the hospital with urethral catheter, for them to attend a Trial Without Catheter (TWOC) clinic at a later date for catheter removal. Traditionally after catheter is removed in the clinic the nurse has to wait for up to 5 hours before the patient get the urge to pass urine and empty the bladder. The main objective of this study is to see the effect of catheter valve on the length of clinic stay (timing of discharge)for the patients (men age 60-85) after catheter is removed. In this study after randomization, patients in Group A (catheter valve group) will be given a catheter valve before they are sent home with the catheter.They will be asked to close the valve 3-4 hours (time required for adequate filling of bladder, which means minimum of 250 mls in bladder with natural filling) before their appointment. It is very likely that by the time these patients are seen in the TWOC clinic their bladder is already full and they will void soon after removal of catheter.The patients in Group B (control) will go home with free drainage catheter and urine bag (standard catheter removal). These patients on arrival, in the TWOC clinic will have an empty bladder when their catheter is removed, they will then drink plenty of fluids in the clinic and wait for their bladder to be full before they void spontaneously. This study will last for one year after approval by ethical committee. The time saved in this process would lessen patient anxiety, lead to more patients being reviewed in clinic and therefore reduced waiting times in TWOC clinics and will save money.
Detailed Description
Men who are discharged from the hospital with urinary catheter in situ are given an appointment to come to trial TWOC (trail without catheter) clinic for removal of their catheters. Purpose and design: In the TWOC clinic their catheters are removed and they usually wait for up to 5 hours hours before they get an urge to pass urine and empty the bladder and then sent home by the nurse. Waiting for up to 5 hours in the clinic reduces patient satisfaction and increases their anxiety. It also keeps the urology nurse busy in the clinic. This is shown by a clinical audit, which has been carried out in our department. The aim of this study is to find out the ways to reduce this waiting time for the patients. In this study catheter valve is used to see if it significantly reduces time spent by the patient in the TWOC clinic after catheter removal. The patients in the catheter valve group are compared to the patients who did not use the valve (this is the standard method which is currently used by most of the TWOC clinics). Catheter valve is a device, which is attached to the end of urinary catheter and can be used easily by any one who has normal manual dexterity and no cognitive impairment. The study proposal was developed by lead urology nurse practitioner and endorsed by the consultant urological surgeons from three different hospitals in Kent UK (Medway Maritime Hospital, Darent Valley Hospital and Maidstone Hospital). Recruitment: Patients will be identified and recruited in the hospital ward. The patients who are planned to go home with the catheter will be provided with the patient information leaflet about his study. They will be given 6 hours to decide if they want to participate in this study. Those patients who agree to participate will be asked to sign a written informed consent. A computer-generated randomisation will be carried out. They will be given a contact number of the urology nurse in case they have any problems or if they want to ask any questions before attending TWOC clinic. A day after discharge urology nurse practitioner will ring the patient at home to check if the patient still wants to participate in this study. A day before their appointment for TWOC clinic urology nurse will ring the patient (in Group A, valve group) to remind him about the appointment and also remind him to close the valve 3-4 hours before appointment time and patients in both groups (Group A and Group B) to drink three glasses of water before coming to the hospital for catheter removal. Patients will be informed that they can withdraw from the study at any point. Inclusion and exclusion: A strict inclusion and exclusion criteria will be observed. Vulnerable men with learning difficulties/dementia/Alzheimer's disease or those with poor manual dexterity will not be included. Consent: Written informed consent will be used after patients has read the patient information leaflet and the study has been verbally explained to the patient by the researchers. Risks, burdens and benefits There is no potential risk to the patients associated with the planned intervention.The vulnerable adults with learning difficulties/Dementia and poor manual dexterity will be excluded. In the intervention arm (GROUP A: patient with valve) the patient may get a pain with strong desire to pass urine or start bypassing catheter much before 3 hours after closing the valve. In this case patients will be instructed to open the valve and drain the urine. (These patients will be excluded). If there is significant reduction (one hour or more) in the time spent in the clinic for the valve group noted in this study that will help in decreasing patient's anxiety, improved efficacy of the TWOC clinic and reduce the cost of running the TWOC clinic. Confidentiality: The data will be recorded electronically and will be saved in a password protected computer. The researchers and statistician can only access it. Conflict of interest: There is no conflict of interest. All the researchers will sign the form.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Retention
Keywords
Urinary retention, trial removal of catheter, valve

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Without valve
Arm Type
Active Comparator
Arm Description
Trial removal of catheter without catheter valve in patients with urinary retention. These are those patients who have catheter on free drainage, attend the clinic for catheter removal and bladder to be filled naturally ( which may take upto 4-5 hours). After removal of catheter they will be asked to drink plenty of fluids while waiting for the bladder to fill up. This is the traditional method of catheter removal.
Arm Title
With valve
Arm Type
Experimental
Arm Description
Trial removal of catheter in patients with urinary retention with closed catheter valve. These patients will be asked to close the valve 3-4 hours before attending the clinic prior to catheter removal. Here the intervention is catheter valve that allows bladder to be comfortably full by the time patient arrives in the clinic. By this intervention the investigators hypothesise that the investigators can save the clinic time as the patient will not need to wait for natural bladder filling which generally takes 4-5 hours. Intervention: Urinary catheter valve
Intervention Type
Procedure
Intervention Name(s)
Use of catheter valve before 'trial removal of catheter'
Intervention Description
The investigators are comparing two groups of patients (Group A) Trial removal of urinary catheter in patients with urinary retention after applying catheter valve and closing it 3-4 hours before catheter removal.
Intervention Type
Procedure
Intervention Name(s)
Trial removal of catheter in patients with urinary retention
Intervention Description
The investigators are comparing two groups of patients (Group B) Trial removal of urinary catheter in patients with urinary retention without using catheter valve - 'Traditional method'
Primary Outcome Measure Information:
Title
Time to spontaneous void after catheter removal
Description
The primary outcome measure of this study is to see if usage of catheter valve results in early spontaneous voiding after catheter removal and thus significantly reduces the time spent by these patients in the clinic.
Time Frame
On the day of catheter removal
Secondary Outcome Measure Information:
Title
Complications associated with valve
Description
To see if the patients with the catheter valve have more complications (catheter bypass, urinary tract infection and pain).
Time Frame
On the day of catheter removal
Title
Reduction in clinic waiting time (hours)
Description
To see if usage of catheter valve results in early discharge after catheter removal resulting in reduction of time spent in the clinic (in hours)
Time Frame
On the day of catheter removal
Title
Reduction in the cost of running the clinic
Description
To see if reduction in the time spent by the catheter valve patients results in reducing the cost of running of the TWOC (Trial without catheter) clinic (in British Pound Sterling).
Time Frame
On the day of catheter removal

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
60 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men aged 60-85 catheterised for urinary retention and booked for outpatient removal of catheter Mobile patients Exclusion Criteria: Who cannot consent Residual urine of more then 1 litre Abnormal renal functions Poor manual dexterity Learning difficulties/dementia.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shikohe Masood, MD
Phone
00441634830000
Ext
3781
Email
shikohemasood@nhs.net
First Name & Middle Initial & Last Name or Official Title & Degree
Robert Hughes, MA
Phone
00441634830000
Ext
3129
Email
robert.hughes@medway.nhs.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shikohe Masood, MD
Organizational Affiliation
Medway NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medway NHS Foundation Trust
City
Gillingham
State/Province
Kent
ZIP/Postal Code
ME7 5NY
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shikohe Masood, MD
Phone
00441634830000
Ext
3871
Email
shikohemasood@nhs.net
First Name & Middle Initial & Last Name & Degree
Robert Hughes, MA
Phone
00441634830000
Ext
3129
Email
robert.hughes@medway.nhs.uk

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
9224329
Citation
Jacobsen SJ, Jacobson DJ, Girman CJ, Roberts RO, Rhodes T, Guess HA, Lieber MM. Natural history of prostatism: risk factors for acute urinary retention. J Urol. 1997 Aug;158(2):481-7. doi: 10.1016/s0022-5347(01)64508-7.
Results Reference
background
PubMed Identifier
9043505
Citation
Lyth DR, Braslis K, Iacovou JW. The infusion trial of micturition. Br J Urol. 1997 Jan;79(1):94-5. doi: 10.1046/j.1464-410x.1997.30520.x.
Results Reference
background
PubMed Identifier
21492377
Citation
Boccola MA, Sharma A, Taylor C, Wong LM, Travis D, Chan S. The infusion method trial of void vs standard catheter removal in the outpatient setting: a prospective randomized trial. BJU Int. 2011 Apr;107 Suppl 3:43-6. doi: 10.1111/j.1464-410X.2011.10044.x.
Results Reference
background
PubMed Identifier
22984818
Citation
Du J, Marshall D, Leyland J, Shaw L, Broome KE, Mason DF. Prospective, multicentre, randomized controlled trial of bladder filling prior to trial of void on the timing of discharge. ANZ J Surg. 2013 Apr;83(4):239-42. doi: 10.1111/j.1445-2197.2012.06253.x. Epub 2012 Sep 18.
Results Reference
background
PubMed Identifier
9439409
Citation
Wilson C, Sandhu SS, Kaisary AV. A prospective randomized study comparing a catheter-valve with a standard drainage system. Br J Urol. 1997 Dec;80(6):915-7. doi: 10.1046/j.1464-410x.1997.00473.x.
Results Reference
background
PubMed Identifier
9043506
Citation
German K, Rowley P, Stone D, Kumar U, Blackford HN. A randomized cross-over study comparing the use of a catheter valve and a leg-bag in urethrally catheterized male patients. Br J Urol. 1997 Jan;79(1):96-8. doi: 10.1046/j.1464-410x.1997.30321.x.
Results Reference
background

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The Effect of Catheter Valve Vs. Standard Catheter Removal in Outpatients

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