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Lithium Therapeutic Drug Monitoring; Once Daily Vs Twice Daily Dosing and the Impact of Kidney Function

Primary Purpose

Bipolar Disorder, Major Depressive Disorder

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Lithium level
Serum Creatinine
Sponsored by
Mount Sinai Hospital, Canada
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bipolar Disorder focused on measuring lithium, pharmacokinetics, renal, kidney

Eligibility Criteria

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

Inclusion Criteria:

  • Adult patients admitted to the inpatient psychiatry unit at Mount Sinai Hospital treated with lithium therapy (i.e. taking lithium before admission, or initiated on lithium therapy during hospitalization)

Exclusion Criteria:

  • any patients who are currently pregnant
  • patients taking lithium three times daily
  • patients taking lithium with a specific dosing frequency for a documented clinical reason.

Sites / Locations

  • Mount Sinai HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Once Daily Dosing

Twice Daily Dosing

Arm Description

In this arm of the study, participants receive the prescribed dose of lithium once daily at bedtime. After 4-6 days, a steady state lithium serum level and serum creatinine are taken, and they crossover to the other arm (twice daily dosing, if they have not already done so). Frequency of selected medication use is noted.

In this arm of the study, participants receive the prescribed dose of lithium divided into two daily doses. After 4-6 days a steady state lithium serum level and serum creatinine are taken, and they crossover to the other arm (once daily dosing, if they have not already done so).Frequency of selected medication use is noted.

Outcomes

Primary Outcome Measures

Difference in lithium levels between once and twice daily dosing
The average of the difference in 12 hour post-dose serum level between the two dosing regimens (once daily and twice daily dosing)

Secondary Outcome Measures

Correlation between renal function and difference in lithium level
Calculated correlation coefficient (r) for renal function (as estimated by calculation of creatinine clearance via Cockroft Gault) and mean percent change in serum lithium concentration when transitioning between once and twice daily dosing
Frequency of selected concurrent medication use
Frequency of thiazide diuretic, loop diuretic, NSAID, and ACE inhibitor/ARB use

Full Information

First Posted
January 10, 2019
Last Updated
March 6, 2019
Sponsor
Mount Sinai Hospital, Canada
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1. Study Identification

Unique Protocol Identification Number
NCT03811860
Brief Title
Lithium Therapeutic Drug Monitoring; Once Daily Vs Twice Daily Dosing and the Impact of Kidney Function
Official Title
Lithium Therapeutic Drug Monitoring; Once Daily Vs Twice Daily Dosing and the Impact of Kidney Function
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Unknown status
Study Start Date
February 6, 2019 (Actual)
Primary Completion Date
September 2019 (Anticipated)
Study Completion Date
December 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mount Sinai Hospital, Canada

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Lithium is a mainstay in the treatment of bipolar disorder, and a frequently used adjunctive therapy for major depressive disorder. It is accepted practice to monitor lithium serum levels to monitor for efficacy and toxicity. However, studies on the difference in lithium levels between once and twice daily dosing, which also assess the impact of kidney function are scarce. The aim of this study is to quantify this pharmacokinetic difference, identify the impact of kidney function, in the context of estimating effects to inform feasibility and sample size needed for a larger well-powered study.
Detailed Description
Bipolar disorder is a chronic and recurring condition which causes functional impairment and increases lifetime suicide risk. Major depressive disorder likewise confers a high burden of illness on the affected population, and treatment is complicated by the fact 50-70% of patients treated with an initial agent do not achieve full remission of symptoms. There are numerous clinical practice guidelines which support the use of lithium as a first-line agent for bipolar disorder, and as an adjunctive therapy for major depressive disorder. Therapeutic ranges for lithium were established in the 1970s using multiple daily dose regimens, and therefore should not be directly applied to patients taking lithium once daily. The current standard of practice is to measure levels 12 hours post dose irrespective of once or twice daily administration. There is some evidence that lithium levels drawn 12 hours post dose are 10 - 26% higher when dosing lithium once daily compared to twice daily, however, the impact of kidney function on this difference has not been studied, and this difference in 12h post levels has not been confirmed via prospective data. Guidance on therapeutic drug monitoring (TDM) is vague with respect to interpretation of specific lithium blood levels for once daily dosing. Physicians may reduce a patient's dose based on a lithium level that is seemingly higher that target, even if the patient is clinically stable, putting the patient at risk for re-emergence of symptoms. Though it is known that lithium is excreted by the kidney, the impact of kidney function on the difference in lithium levels when dosed once daily compared to twice daily is not well understood. The results of this pilot study will help identify the impact of kidney function on lithium therapeutic drug monitoring in current practice, and potentially lead to a larger multi-center study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder, Major Depressive Disorder
Keywords
lithium, pharmacokinetics, renal, kidney

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
15 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Once Daily Dosing
Arm Type
Active Comparator
Arm Description
In this arm of the study, participants receive the prescribed dose of lithium once daily at bedtime. After 4-6 days, a steady state lithium serum level and serum creatinine are taken, and they crossover to the other arm (twice daily dosing, if they have not already done so). Frequency of selected medication use is noted.
Arm Title
Twice Daily Dosing
Arm Type
Active Comparator
Arm Description
In this arm of the study, participants receive the prescribed dose of lithium divided into two daily doses. After 4-6 days a steady state lithium serum level and serum creatinine are taken, and they crossover to the other arm (once daily dosing, if they have not already done so).Frequency of selected medication use is noted.
Intervention Type
Diagnostic Test
Intervention Name(s)
Lithium level
Intervention Description
The level of lithium in the serum
Intervention Type
Diagnostic Test
Intervention Name(s)
Serum Creatinine
Intervention Description
The level of creatinine (as an indicator of kidney function, to approximate GFR) in the serum
Primary Outcome Measure Information:
Title
Difference in lithium levels between once and twice daily dosing
Description
The average of the difference in 12 hour post-dose serum level between the two dosing regimens (once daily and twice daily dosing)
Time Frame
once 2 steady state levels have been taken (4-12 days of intervention)
Secondary Outcome Measure Information:
Title
Correlation between renal function and difference in lithium level
Description
Calculated correlation coefficient (r) for renal function (as estimated by calculation of creatinine clearance via Cockroft Gault) and mean percent change in serum lithium concentration when transitioning between once and twice daily dosing
Time Frame
once 2 steady state levels have been taken (4-12 days of intervention) and average creatinine clearance has been calculated
Title
Frequency of selected concurrent medication use
Description
Frequency of thiazide diuretic, loop diuretic, NSAID, and ACE inhibitor/ARB use
Time Frame
recorded upon enrollment, and every 4-6 days until study completion, up to 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients admitted to the inpatient psychiatry unit at Mount Sinai Hospital treated with lithium therapy (i.e. taking lithium before admission, or initiated on lithium therapy during hospitalization) Exclusion Criteria: any patients who are currently pregnant patients taking lithium three times daily patients taking lithium with a specific dosing frequency for a documented clinical reason.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Virginia Fernandes, PharmD
Phone
416-586-4800
Email
virginia.fernandes@sinaihealthsystem.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Dario A Moscoso, PharmD
Phone
416-586-4800
Email
dario.moscoso@sinaihealthsystem.ca
Facility Information:
Facility Name
Mount Sinai Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 1X5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Virginia Fernandes, PharmD

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There is no such plan

Learn more about this trial

Lithium Therapeutic Drug Monitoring; Once Daily Vs Twice Daily Dosing and the Impact of Kidney Function

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