search
Back to results

GAG Replacement vs URethral DIlAtatioN (GUARDIAN)

Primary Purpose

Recurrent Urinary Tract Infection

Status
Withdrawn
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Rigid cystoscopy with urethral dilatation
Flexible cystoscopy and installation of Glycosaminoglycan layer replacement (laluril)
Sponsored by
Hampshire Hospitals NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Recurrent Urinary Tract Infection

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Female
  2. Pre-menopausal 3 - 3 episodes of cystitis in the last 12 months as defined by:

    1. 3 symptoms from dysuria, frequency, urgency, suprapubic tenderness, haematuria, polyuria
    2. Or less than 2 symptoms from the above list, but with cloudy urine 4 - Normal flow studies with bladder residual <150ml 5 - Normal renal tract on USS

Exclusion Criteria:

  1. - Anatomical anomalies of urinary tract
  2. - Neurological condition
  3. - Diabetes mellitus
  4. - Pregnancy
  5. - Use of Immunosuppressants
  6. - Symptomatic of UTI at time of treatment

Sites / Locations

  • Hampshire Hospitals NHS Foundation Trust

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Rigid Cystoscopy and Urethral dilatation

Flexible cystoscopy and Glycosaminoglycan Layer replacement

Arm Description

Rigid cystoscopy, performed under General Anaesthetic, followed by intervention of urethral dilatation with Hagar dilators.

Flexible cystoscopy, under Local Anaesthetic, followed by the intervention, which is 6 installations of Ialuril (a Glycosaminoglycan Layer replacement)

Outcomes

Primary Outcome Measures

The number of Urinary tract infections in the 12 months following treatment
Number of symptomatic UTI episodes in 12 months following treatment

Secondary Outcome Measures

The time to first urinary tract infection after completion of treatment.
Time (in days) to first symptomatic UTI episode after completion of treatment.
The change in the Quality of life (QoL) between the time of treatment and at 3, 6 and 12 months following initiation of treatment.
Following treatment is there any recorded change in the QoL questionnaire (SF-12) score from pre-treatment baseline
The number of adverse events recorded following treatment during the 12-month study period
A record of the number, recorded in groups by their nature, of adverse events following treatment during the 12 month study.
The change in the Patient Satisfaction at 3, 6 and 12 months following initiation of treatment
Following treatment is there any recorded change in the Patient Satisfaction report from pre-treatment baseline
The change in female sexual function index (FSFI) questionnaire at 3, 6 and 12 months
Following treatment is there any recorded change in the FSFI questionnaire score (out of 36) from pre-treatment baseline
The change in Hospital anxiety and depression scale (HADS) questionnaire at 3, 6 and 12 months
Following treatment is there any recorded change in the HADS questionnaire score (out of 21 for anxiety and 21 for depression) from pre-treatment baseline

Full Information

First Posted
May 3, 2018
Last Updated
September 21, 2021
Sponsor
Hampshire Hospitals NHS Foundation Trust
search

1. Study Identification

Unique Protocol Identification Number
NCT03861260
Brief Title
GAG Replacement vs URethral DIlAtatioN
Acronym
GUARDIAN
Official Title
To Investigate and Compare The Efficacy of Urethral Dilatation Versus Glycosaminoglycan Layer Replacement in The Management Of Women With Recurrent Urinary Tract Infections
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Withdrawn
Why Stopped
Withdrawn no participants enrolled
Study Start Date
April 30, 2019 (Actual)
Primary Completion Date
October 28, 2019 (Actual)
Study Completion Date
October 28, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hampshire Hospitals NHS Foundation Trust

4. Oversight

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

5. Study Description

Brief Summary
The aim of this randomised parallel trial is to compare the efficacy of Glycosaminoglycan layer replacement against cystoscopy and urethral dilatation in the treatment of recurrent urinary tract infection in pre-menopausal women. The women will be randomised to 1 of 2 arms.Arm 1 patients will receive standard treatment from the Urologists. This will involve rigid cystoscopy and urethral dilatation, under general anaesthetic. Arm 2 patients will receive standard treatment from the Gynaecologists.
Detailed Description
Recurrence of a Urinary Tract Infection (UTI) is defined as infection, following complete resolution of a previous UTI.Recurrent UTI (rUTI) is defined as 3 or more microbiologically confirmed UTI within 12 months. rUTI is an economic problem for healthcare services. rUTI is also detrimental to the quality of life (QoL) of women who suffer the disease. 61% of women who suffer rUTI report symptoms of depression and an associated decrease in their reported QoL scores. QoL was found to improve significantly with successful treatment. E-coli is the most common bacteria causing UTI and 10% are thought to be antibiotic resistant. Consequently, new treatment strategies are required. The Glycosaminoglycans (GAG) layer is thought to be instrumental as a defence mechanism against uro-pathogens. GAG's are polysaccharides forming a gel like substance on the apical surface of the bladder wall and act as a barrier to uro-pathogens. There is now strong evidence that a reduction in the impermeability of the GAG layer is linked to rUTI. Urethral dilatation is an alternative treatment to GAG replacement in the management of rUTI. It is a treatment option more widely adopted by Urologists, although there is a paucity of data to support its use. Currently there is no standardised strategy for the management of women with rUTI. Treatments vary between GAG layer replacement (intravessical therapy with hyaluronic acid and chondroitin sulphate) or a cystoscopy and urethral dilatation. Evidence for each regime varies greatly and is of poor quality. This is a randomised study comparing GAG layer replacement with cystoscopy and urethral dilatation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recurrent Urinary Tract Infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Rigid Cystoscopy and Urethral dilatation
Arm Type
Other
Arm Description
Rigid cystoscopy, performed under General Anaesthetic, followed by intervention of urethral dilatation with Hagar dilators.
Arm Title
Flexible cystoscopy and Glycosaminoglycan Layer replacement
Arm Type
Other
Arm Description
Flexible cystoscopy, under Local Anaesthetic, followed by the intervention, which is 6 installations of Ialuril (a Glycosaminoglycan Layer replacement)
Intervention Type
Procedure
Intervention Name(s)
Rigid cystoscopy with urethral dilatation
Intervention Description
Patients will have a general anaesthetic and a rigid cytoscopic examination of the bladder dilated with sterile water. The urethra will be dilated from FR20 in incremental diameter increases of 2 to French 32 if possible.
Intervention Type
Procedure
Intervention Name(s)
Flexible cystoscopy and installation of Glycosaminoglycan layer replacement (laluril)
Intervention Description
Patients will undergo flexible cystoscopy and intravesical installations of Hyaluronic acid (HA) + Chondroitin Sulphate (CS) (GAGs) weekly for 4 weeks and then at 8 weeks and 12 weeks.
Primary Outcome Measure Information:
Title
The number of Urinary tract infections in the 12 months following treatment
Description
Number of symptomatic UTI episodes in 12 months following treatment
Time Frame
12 months
Secondary Outcome Measure Information:
Title
The time to first urinary tract infection after completion of treatment.
Description
Time (in days) to first symptomatic UTI episode after completion of treatment.
Time Frame
12 month study period
Title
The change in the Quality of life (QoL) between the time of treatment and at 3, 6 and 12 months following initiation of treatment.
Description
Following treatment is there any recorded change in the QoL questionnaire (SF-12) score from pre-treatment baseline
Time Frame
3, 6 and 12 months
Title
The number of adverse events recorded following treatment during the 12-month study period
Description
A record of the number, recorded in groups by their nature, of adverse events following treatment during the 12 month study.
Time Frame
12 months
Title
The change in the Patient Satisfaction at 3, 6 and 12 months following initiation of treatment
Description
Following treatment is there any recorded change in the Patient Satisfaction report from pre-treatment baseline
Time Frame
3, 6 and 12 months
Title
The change in female sexual function index (FSFI) questionnaire at 3, 6 and 12 months
Description
Following treatment is there any recorded change in the FSFI questionnaire score (out of 36) from pre-treatment baseline
Time Frame
3, 6 and 12 months
Title
The change in Hospital anxiety and depression scale (HADS) questionnaire at 3, 6 and 12 months
Description
Following treatment is there any recorded change in the HADS questionnaire score (out of 21 for anxiety and 21 for depression) from pre-treatment baseline
Time Frame
3, 6 and 12 months

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Female Pre-menopausal 3 - 3 episodes of cystitis in the last 12 months as defined by: 3 symptoms from dysuria, frequency, urgency, suprapubic tenderness, haematuria, polyuria Or less than 2 symptoms from the above list, but with cloudy urine 4 - Normal flow studies with bladder residual <150ml 5 - Normal renal tract on USS Exclusion Criteria: - Anatomical anomalies of urinary tract - Neurological condition - Diabetes mellitus - Pregnancy - Use of Immunosuppressants - Symptomatic of UTI at time of treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christian Phillips, MBBS MD
Organizational Affiliation
Hampshire Hospitals NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hampshire Hospitals NHS Foundation Trust
City
Basingstoke
State/Province
Hampshire
ZIP/Postal Code
RG24 9NA
Country
United Kingdom

12. IPD Sharing Statement

Learn more about this trial

GAG Replacement vs URethral DIlAtatioN

We'll reach out to this number within 24 hrs