D-mannose for the Prevention of UTIs in Multiple Sclerosis
Primary Purpose
Multiple Sclerosis, Recurrent Urinary Tract Infections
Status
Unknown status
Phase
Phase 1
Locations
United Kingdom
Study Type
Interventional
Intervention
D Mannose
Sponsored by
About this trial
This is an interventional prevention trial for Multiple Sclerosis focused on measuring D mannose, multiple sclerosis, recurrent urinary infections
Eligibility Criteria
Inclusion Criteria:
- Patients with a known diagnosis of Multiple sclerosis (all stages) who have been clinically stable for at least three months and reporting lower urinary tract symptoms.
- Patient with recurrent urinary tract infections, defined as having at least two urinary tract infections in the preceding six months or three or more urinary tract infections in the preceding one year. Urinary tract infections were defined retrospectively by patient self-report and confirmation by urine culture.
- Age over 18 years and below 65
- Females of childbearing potential using effective contraception if sexually active - oral contraceptive pill (> 3 months use), condoms, intrauterine contraceptive device, depot injection
Exclusion Criteria:
- Pregnancy or planning pregnancy
- Breastfeeding
- History of congenital urinary tract anomalies or interstitial cystitis
- History of diabetes mellitus
- Receiving antibiotic prophylaxis or cranberry extract preparations
- Current urinary tract infection
- Current vaginal infection
- Any known allergies to D-mannose
Sites / Locations
- The National Hospital for Neurology and NeurosurgeryRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
MS and rec UTIs not using a catheter
MS and rec UTIs using a catheter
Arm Description
people with multiple sclerosis and recurrent urinary tract infections with spontaneous voiding Intervention- will be given D-mannose
people with multiple sclerosis and recurrent urinary tract infections using either urethral or suprapubic indwelling catheter or intermittent catheterisation Intervention- will be given D-mannose
Outcomes
Primary Outcome Measures
Compliance (self-usage diary and weight of returned containers of D-mannose)
Compliance to a 16-week course of D-mannose as assessed using a self-usage diary and weight of returned containers of D-mannose. The number of days the participant does not use D-mannose and reasons for non-use will be noted.
Secondary Outcome Measures
Antibiotic prescription (Number of prescriptions for antibiotics required)
Number of prescriptions for antibiotics required during the 16-week course
Full Information
NCT ID
NCT02490046
First Posted
April 28, 2015
Last Updated
July 1, 2015
Sponsor
University College, London
Collaborators
UCLH
1. Study Identification
Unique Protocol Identification Number
NCT02490046
Brief Title
D-mannose for the Prevention of UTIs in Multiple Sclerosis
Official Title
Single Centre Open-label Feasibility Study Evaluating the Use of D-mannose in Multiple Sclerosis
Study Type
Interventional
2. Study Status
Record Verification Date
July 2015
Overall Recruitment Status
Unknown status
Study Start Date
February 2015 (undefined)
Primary Completion Date
October 2015 (Anticipated)
Study Completion Date
November 2015 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University College, London
Collaborators
UCLH
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This is a study to explore the feasibility of using D-mannose, a commonly used food supplement, in persons with multiple sclerosis reporting recurrent urinary tract infections. Twenty persons with multiple sclerosis (10 patients using catheters and 10 not using catheters) reporting recurrent urinary tract infections will receive D-mannose 1.5 grams twice daily for 16 weeks duration.
This will be explored through:
Assessing compliance to a 16-week course of D-mannose
Quantifying the number of prescriptions for antibiotics during the 16 weeks course of D-mannose
Detailed Description
Informed consent procedure: Potential participants will be approached in clinic and given a patient information sheet and adequate time will be given for the individual to read through the patient information sheet and for clarification of any queries or concerns. Informed consent will be obtained by one of the investigators involved in the conduct of the study prior to participation in the trial, following adequate explanation of the aims, methods, anticipated benefits and potential hazards of the study.
Screening Period: Before any screening procedures occur, participants will sign an Informed Consent Form.
During the screening evaluation the following procedures will be conducted and recorded for all patients:
Informed Consent
Evaluation of compliance with inclusion and exclusion criteria
Demography and Past Medical History
Vital signs including weight
Physical examination including neurological examination
Review of concomitant medications
Baseline assessments: A urine sample will be tested for an infection using Urine multistix in the Department of Uro-neurology, which is a routine clinical practice. Participants will enter a discussion about the symptoms of a urinary tract infection and be taught the use of Urine multistix. They will complete standardised validated questionnaires for overactive bladder syndrome (ICIQ-OAB, sf-Qualiveen® and EQ5D-5L™).
Treatment procedures: Patients will receive D-mannose powder to be used 1.5 gm (one level-teaspoon) twice daily, to be added to any beverage, for 16 weeks. D-mannose is classed as a food supplement and is widely available in the United Kingdom for purchase. D-Mannose will be sourced from D-Mannose Limited.
Subsequent assessments: Compliance will be assessed by using a Usage diary, on which the use of D-mannose will be marked and any problems noted. Acceptability and tolerability to D-mannose will be assessed through the diary. Additionally, patients will be phoned after one week, and after 8 weeks, to enquire about well-being and compliance.
Participants will be asked to note the number of prescriptions they receive during the 16 week course in a urinary tract infection diary. Suspected self-reported urinary tract infections will be noted in a diary, as well as the results of the urine multistix. Standard clinical practice will be followed and participants with a suspected urinary tract infection will inform their general practitionner, mid-stream urine samples sent to the lab and antibiotic treatment started. Patients will continue to take D-mannose. The usage diary has to be sent by the patients every week.
At week 16, patients will be asked to return for a second visit. Compliance and urinary tract infection diaries will be collected and reviewed. They will be asked to complete questionnaires (ICIQ-OAB, sf-Qualiveen® and EQ5D-5L™) and neurological status will be evaluated.
The study will be conducted in accordance with the International Conference on Harmonization Good Clinical Practice guidelines and the Declaration of Helsinki, and within local laws and regulations.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis, Recurrent Urinary Tract Infections
Keywords
D mannose, multiple sclerosis, recurrent urinary infections
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
MS and rec UTIs not using a catheter
Arm Type
Experimental
Arm Description
people with multiple sclerosis and recurrent urinary tract infections with spontaneous voiding Intervention- will be given D-mannose
Arm Title
MS and rec UTIs using a catheter
Arm Type
Experimental
Arm Description
people with multiple sclerosis and recurrent urinary tract infections using either urethral or suprapubic indwelling catheter or intermittent catheterisation Intervention- will be given D-mannose
Intervention Type
Dietary Supplement
Intervention Name(s)
D Mannose
Intervention Description
Patients in both arms will receive D-mannose powder to be used 1.5 gm (one level-teaspoon) twice daily, to be added to any beverage, for 16 weeks.
Primary Outcome Measure Information:
Title
Compliance (self-usage diary and weight of returned containers of D-mannose)
Description
Compliance to a 16-week course of D-mannose as assessed using a self-usage diary and weight of returned containers of D-mannose. The number of days the participant does not use D-mannose and reasons for non-use will be noted.
Time Frame
16 weeks
Secondary Outcome Measure Information:
Title
Antibiotic prescription (Number of prescriptions for antibiotics required)
Description
Number of prescriptions for antibiotics required during the 16-week course
Time Frame
16 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with a known diagnosis of Multiple sclerosis (all stages) who have been clinically stable for at least three months and reporting lower urinary tract symptoms.
Patient with recurrent urinary tract infections, defined as having at least two urinary tract infections in the preceding six months or three or more urinary tract infections in the preceding one year. Urinary tract infections were defined retrospectively by patient self-report and confirmation by urine culture.
Age over 18 years and below 65
Females of childbearing potential using effective contraception if sexually active - oral contraceptive pill (> 3 months use), condoms, intrauterine contraceptive device, depot injection
Exclusion Criteria:
Pregnancy or planning pregnancy
Breastfeeding
History of congenital urinary tract anomalies or interstitial cystitis
History of diabetes mellitus
Receiving antibiotic prophylaxis or cranberry extract preparations
Current urinary tract infection
Current vaginal infection
Any known allergies to D-mannose
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jalesh Panicker, MD, FRCP
Phone
0203 448 4713
Email
j.panicker@ucl.ac.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Véronique Phé, MD
Phone
0203 448 4713
Email
Veronique.Phe@uclh.nhs.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jalesh Panicker, MD,FRCP
Organizational Affiliation
UCLH NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
The National Hospital for Neurology and Neurosurgery
City
London
ZIP/Postal Code
WC1N 3BG
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jalesh Panicker, MD, FRCP
Phone
020 344 84713
Email
j.panicker@ucl.ac.uk
First Name & Middle Initial & Last Name & Degree
Véronique Phé, MD
Phone
020 344 84713
Email
Veronique.Phe@uclh.nhs.uk
First Name & Middle Initial & Last Name & Degree
Mahreen Pakzad, FRCS
First Name & Middle Initial & Last Name & Degree
Jalesh Panicker, MD, FRCP
First Name & Middle Initial & Last Name & Degree
Véronique Phé, MD
12. IPD Sharing Statement
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D-mannose for the Prevention of UTIs in Multiple Sclerosis
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