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High Water Intake in Polycystic Kidney Disease (DRINK)

Primary Purpose

Autosomal Dominant Polycystic Kidney Disease

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
High water intake
Ad libitum water intake
Sponsored by
Cambridge University Hospitals NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Autosomal Dominant Polycystic Kidney Disease focused on measuring Autosomal Dominant Polycystic Kidney Disease, Polycystic Kidney Disease, ADPKD, Water, Vasopressin, Dietary

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Have given written informed consent to participate
  • Aged 16 years or older
  • Have a diagnosis of ADPKD (fulfilling radiological diagnostic criteria ± genetic evidence)
  • eGFR ≥ 20ml/min/1.73m2
  • Able to self-monitor urine SG

Exclusion Criteria:

  • Inability to provide informed consent
  • eGFR < 20ml/min/1.73m2
  • Fluid overload states e.g. heart failure, cirrhosis, or requirement for fluid restriction
  • Confounding illness impacting on renal disease e.g. concomitant diabetes or glomerulonephritis
  • Treatment with diuretics for fluid overload (those on diuretics for hypertension may participate in the trial after a run-in period of 2 weeks)
  • Treatment with Tolvaptan in the last 4 weeks
  • Pregnancy or breastfeeding

Sites / Locations

  • Cambridge University Hospitals NHS Foundation Trust

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Ad libitum water intake

High water intake

Arm Description

Ad libitum water intake, defined as intake guided by thirst to achieve a target urine osmolality > 300 mOsmo/kg

Personalised daily water intake prescription to achieve target urine osmolality < 270 mOsm/kg.

Outcomes

Primary Outcome Measures

The proportion of patients achieving a urine osmolality < 270 mOsm/kg

Secondary Outcome Measures

Urine osmolality
Achieved urine osmolality as a surrogate for vasopressin suppression
Proportion of participants that can self-monitor and report urine specific gravity reliably
Proportion of patients experiencing a serious adverse event
Acute change in estimated GFR
Evaluation of the change form baseline eGFR after 2 weeks
Health-Related Quality of Life (HRQoL)
Change from baseline HRQoL as estimated by EQ5D-5L
Recruitment rate

Full Information

First Posted
September 18, 2016
Last Updated
January 13, 2019
Sponsor
Cambridge University Hospitals NHS Foundation Trust
Collaborators
PKD Charity, Addenbrookes Charitable Trust, British Renal Society & British Kidney Patient Association
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1. Study Identification

Unique Protocol Identification Number
NCT02933268
Brief Title
High Water Intake in Polycystic Kidney Disease
Acronym
DRINK
Official Title
Determining Feasibility of Randomisation to High vs ad Libitum Water Intake in Polycystic Kidney Disease: The DRINK Randomised Feasibility Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
September 26, 2016 (Actual)
Primary Completion Date
March 31, 2018 (Actual)
Study Completion Date
July 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cambridge University Hospitals NHS Foundation Trust
Collaborators
PKD Charity, Addenbrookes Charitable Trust, British Renal Society & British Kidney Patient Association

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
DRINK is an open-label randomised controlled feasibility trial of high versus ad libitum water intake in ADPKD.
Detailed Description
Autosomal Dominant Polycystic Kidney Disease (PKD) affects 12.5 million people worldwide, and accounts for 7% of those requiring renal replacement therapy. The hormone vasopressin drives cyst growth until ultimately most of the normal functioning kidney tissue is replaced and compressed by cysts over the life course. Half of those affected will require dialysis by the age of 55 years. Vasopressin blockade has emerged as a viable strategy for altering disease course. High water intake suppresses vasopressin, and may therefore slow cyst growth and consequent disease progression. However, evidence to support high water intake in PKD is lacking, and it is not clear whether patients can adhere sufficiently to a high water intake. DRINK is a single-centre prospective, open label, parallel group randomised controlled feasibility trial. The primary objective is to establish whether a definitive large randomised trial comparing high versus ad libitum water intake on long-term disease progression is deliverable. Fifty patients will be recruited from the Renal Genetics service at Addenbrooke's Hospital. Participants will be randomly allocated to the high water intake (high) or the ad libitum (standard) water intake group. For the high intake group the aim is to drink large enough volumes of water to achieve and maintain dilute urine (urine osmolality < 270 mOsmo/kg or urine specific gravity ≤ 1.010 ). Multiple methods will be employed to promote adherence these include instruction and education as well as self-monitoring of urine specific gravity twice weekly by participants and the recording of results via a trial specific smartphone application.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Autosomal Dominant Polycystic Kidney Disease
Keywords
Autosomal Dominant Polycystic Kidney Disease, Polycystic Kidney Disease, ADPKD, Water, Vasopressin, Dietary

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Ad libitum water intake
Arm Type
Active Comparator
Arm Description
Ad libitum water intake, defined as intake guided by thirst to achieve a target urine osmolality > 300 mOsmo/kg
Arm Title
High water intake
Arm Type
Active Comparator
Arm Description
Personalised daily water intake prescription to achieve target urine osmolality < 270 mOsm/kg.
Intervention Type
Dietary Supplement
Intervention Name(s)
High water intake
Intervention Description
High water intake aimed at achieving an urine osmolality < 270mOsmo/kg. Individualised prescription for each participant based on the free water clearance formula calculation.
Intervention Type
Other
Intervention Name(s)
Ad libitum water intake
Intervention Description
Water intake guided by thirst
Primary Outcome Measure Information:
Title
The proportion of patients achieving a urine osmolality < 270 mOsm/kg
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Urine osmolality
Description
Achieved urine osmolality as a surrogate for vasopressin suppression
Time Frame
8 weeks
Title
Proportion of participants that can self-monitor and report urine specific gravity reliably
Time Frame
8 weeks
Title
Proportion of patients experiencing a serious adverse event
Time Frame
12 weeks
Title
Acute change in estimated GFR
Description
Evaluation of the change form baseline eGFR after 2 weeks
Time Frame
4 weeks
Title
Health-Related Quality of Life (HRQoL)
Description
Change from baseline HRQoL as estimated by EQ5D-5L
Time Frame
12 weeks
Title
Recruitment rate
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Have given written informed consent to participate Aged 16 years or older Have a diagnosis of ADPKD (fulfilling radiological diagnostic criteria ± genetic evidence) eGFR ≥ 20ml/min/1.73m2 Able to self-monitor urine SG Exclusion Criteria: Inability to provide informed consent eGFR < 20ml/min/1.73m2 Fluid overload states e.g. heart failure, cirrhosis, or requirement for fluid restriction Confounding illness impacting on renal disease e.g. concomitant diabetes or glomerulonephritis Treatment with diuretics for fluid overload (those on diuretics for hypertension may participate in the trial after a run-in period of 2 weeks) Treatment with Tolvaptan in the last 4 weeks Pregnancy or breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas F Himestra
Organizational Affiliation
Cambridge University Hospital NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cambridge University Hospitals NHS Foundation Trust
City
Cambridge
ZIP/Postal Code
CB2 0QQ
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Yes
Citations:
PubMed Identifier
29743334
Citation
El-Damanawi R, Lee M, Harris T, Mader LB, Bond S, Pavey H, Sandford RN, Wilkinson IB, Burrows A, Woznowski P, Ben-Shlomo Y, Karet Frankl FE, Hiemstra TF. Randomised controlled trial of high versus ad libitum water intake in patients with autosomal dominant polycystic kidney disease: rationale and design of the DRINK feasibility trial. BMJ Open. 2018 May 9;8(5):e022859. doi: 10.1136/bmjopen-2018-022859.
Results Reference
derived

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High Water Intake in Polycystic Kidney Disease

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