Effects of GLP-1 Analogues on Fluid Intake in Patients With Primary Polydipsia (The GOLD-Study) (GOLD)
Primary Purpose
Primary Polydipsia
Status
Completed
Phase
Phase 2
Locations
Switzerland
Study Type
Interventional
Intervention
Dulaglutide
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Primary Polydipsia
Eligibility Criteria
Inclusion Criteria:
- Age over 18 years
- Polyuria of > 50 ml/Kg/day
- Polydipsia of > 3 liters/day
Exclusion Criteria:
- Known or probable central or nephrogenic Diabetes insipidus, expected from patient's history
- Polyuria secondary to diabetes mellitus, hypokalemia, hypercalcemia
- Pregnancy
- Previous treatment with GLP-1 agonists within the last 3 month
- History of pancreatitis
- Severe renal insufficiency (eGFR (CKD EPI) <30 ml/min/1,73 m2)
- Cancer
Sites / Locations
- University Hospital Basel
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Verum first
Placebo first
Arm Description
Dulaglutide (Trulicity®) 1.5 mg in 0.5 ml, via Pen s.c. once weekly for 3 weeks.
Placebo: 0.5 ml normal saline (0.9% sodium chloride [0.9% sodium chloride (NaCl)]), injection sc via syringe once weekly for 3 weeks.
Outcomes
Primary Outcome Measures
Fluid intake in ml
Fluid intake (ml) during an evaluation visit of 8 hours
Secondary Outcome Measures
Quality of Life Assessment using the Short Form-12 (SF-12) Questionnaire
To assess the influence of dulaglutide on thirst perception and quality of life in patients with primary polydipsia compared to placebo.
24h-urine production
24h-urine production in ml during evaluation visit and thereafter
Plasma- and urine osmolality
influence of dulaglutide on osmolality during evaluation visit
Circadian serum- and salivary cortisol levels
Influence of dulaglutide on hypothalamic-pituitary-adrenal axis (HPA axis) activity
Cortisol levels basal and stimulated
Influence of dulaglutide on hypothalamic-pituitary-adrenal axis (HPA axis) activity
Copeptin level
Influence of dulaglutide on copeptin levels after a period of water deprivation
Influence of dulaglutide on neuronal changes
Neuronal changes assessed with a functional magnet resonance Imaging between dulaglutide and Placebo Treatment in a subgroup of patients with primary polydipsia
Neuronal changes between patients with primary polydipsia and healthy volunteers
Differences in neuronal changes assessed by functional magnet resonance imaging
Thirst perception
Influence of dulaglutide on thirst perception
Full Information
NCT ID
NCT02770885
First Posted
March 30, 2016
Last Updated
January 16, 2020
Sponsor
University Hospital, Basel, Switzerland
1. Study Identification
Unique Protocol Identification Number
NCT02770885
Brief Title
Effects of GLP-1 Analogues on Fluid Intake in Patients With Primary Polydipsia (The GOLD-Study)
Acronym
GOLD
Official Title
Effects of GLP-1 Analogues on Fluid Intake in Patients With Primary Polydipsia: "The GOLD-Study"
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
March 2016 (undefined)
Primary Completion Date
May 17, 2019 (Actual)
Study Completion Date
October 7, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Basel, Switzerland
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Glucagon like Peptide -1 (GLP-1) receptor agonists are well known to stimulate glucose-induced insulin secretion and to reduce energy intake. Recent findings from animal and human studies suggest a role of GLP-1 in regulating water and salt homeostasis. GLP-1 has been shown to reduce fluid intake after an oral salt load or during a meal - pointing to a hypodipsic effect. The aim of this study is to elucidate whether these putative hypodipsic properties of GLP-1 might be of advantage in persons with an exaggerated thirst perception as is the case in patients with primary polydipsia.
Detailed Description
GLP-1 analogues are currently used for the treatment of hyperglycaemia associated with type 2 diabetes mellitus and given his properties as a natural satiety hormone, the GLP-1 analogue liraglutide was recently approved by the FDA for weight management.
In studies related to the influence of GLP-1 and -analogues in controlling food intake a concomitant reduction of fluid consumption has been observed.
The investigators hypothesize that GLP-1 analogues not only modulate appetite and provide satiety but also reduce fluid intake and thirst sensation in humans - especially in those with excessive thirst perception (patients with primary polydipsia). In view of future therapeutic options for these patients we aim to investigate the influence of the long-acting GLP-1 analogue dulaglutide on fluid intake, thirst perception and quality of life in patients with primary polydipsia compared to placebo.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Primary Polydipsia
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Verum first
Arm Type
Experimental
Arm Description
Dulaglutide (Trulicity®) 1.5 mg in 0.5 ml, via Pen s.c. once weekly for 3 weeks.
Arm Title
Placebo first
Arm Type
Placebo Comparator
Arm Description
Placebo: 0.5 ml normal saline (0.9% sodium chloride [0.9% sodium chloride (NaCl)]), injection sc via syringe once weekly for 3 weeks.
Intervention Type
Drug
Intervention Name(s)
Dulaglutide
Other Intervention Name(s)
Trulicity
Intervention Description
Treatment with dulaglutide for 3 weeks.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Sodium Chloride 0.9%
Intervention Description
Treatment with Sodium Chloride 0.9% (Placebo) for 3 weeks.
Primary Outcome Measure Information:
Title
Fluid intake in ml
Description
Fluid intake (ml) during an evaluation visit of 8 hours
Time Frame
8 hours
Secondary Outcome Measure Information:
Title
Quality of Life Assessment using the Short Form-12 (SF-12) Questionnaire
Description
To assess the influence of dulaglutide on thirst perception and quality of life in patients with primary polydipsia compared to placebo.
Time Frame
During phase a and b, 3 weeks each
Title
24h-urine production
Description
24h-urine production in ml during evaluation visit and thereafter
Time Frame
24 hours
Title
Plasma- and urine osmolality
Description
influence of dulaglutide on osmolality during evaluation visit
Time Frame
change during evaluation visit of 8 hours
Title
Circadian serum- and salivary cortisol levels
Description
Influence of dulaglutide on hypothalamic-pituitary-adrenal axis (HPA axis) activity
Time Frame
circadian rhythm assessed at timepoints 8am, 12am, 4pm, 8pm and 12pm
Title
Cortisol levels basal and stimulated
Description
Influence of dulaglutide on hypothalamic-pituitary-adrenal axis (HPA axis) activity
Time Frame
Cortisol at timepoint 0 and after 20-30 minutes after synacthen injection
Title
Copeptin level
Description
Influence of dulaglutide on copeptin levels after a period of water deprivation
Time Frame
at begin of evaluation 1 day visit after an overnight fast (no drink, no food)
Title
Influence of dulaglutide on neuronal changes
Description
Neuronal changes assessed with a functional magnet resonance Imaging between dulaglutide and Placebo Treatment in a subgroup of patients with primary polydipsia
Time Frame
during phase a and b, 3rd week each for 15 patients
Title
Neuronal changes between patients with primary polydipsia and healthy volunteers
Description
Differences in neuronal changes assessed by functional magnet resonance imaging
Time Frame
for patients during phase a and b, 3rd week each for 15 patients, 15 matched healthy control subjects
Title
Thirst perception
Description
Influence of dulaglutide on thirst perception
Time Frame
during phase a and b, 3 weeks each and change during evaluation visit of 8 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age over 18 years
Polyuria of > 50 ml/Kg/day
Polydipsia of > 3 liters/day
Exclusion Criteria:
Known or probable central or nephrogenic Diabetes insipidus, expected from patient's history
Polyuria secondary to diabetes mellitus, hypokalemia, hypercalcemia
Pregnancy
Previous treatment with GLP-1 agonists within the last 3 month
History of pancreatitis
Severe renal insufficiency (eGFR (CKD EPI) <30 ml/min/1,73 m2)
Cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mirjam Christ-Crain, Prof
Organizational Affiliation
University Hospital of Basel
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Basel
City
Basel
Country
Switzerland
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
35134170
Citation
Vukajlovic T, Sailer CO, Asmar A, Jensen BL, Vogt DR, Christ-Crain M, Winzeler B. Effect of a 3-Week Treatment with GLP-1 Receptor Agonists on Vasoactive Hormones in Euvolemic Participants. J Clin Endocrinol Metab. 2022 May 17;107(6):e2581-e2589. doi: 10.1210/clinem/dgac063.
Results Reference
derived
PubMed Identifier
34473645
Citation
Winzeler B, Sailer CO, Coynel D, Zanchi D, Vogt DR, Urwyler SA, Refardt J, Christ-Crain M. A randomized controlled trial of the GLP-1 receptor agonist dulaglutide in primary polydipsia. J Clin Invest. 2021 Oct 15;131(20):e151800. doi: 10.1172/JCI151800.
Results Reference
derived
Learn more about this trial
Effects of GLP-1 Analogues on Fluid Intake in Patients With Primary Polydipsia (The GOLD-Study)
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