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Status unknownNCT03811860Updated Mar 8, 2019

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

An interventional study of Lithium level and Serum Creatinine in Bipolar Disorder and Major Depressive Disorder, sponsored by Mount Sinai Hospital, Canada. Status unknown at 1 site in Canada. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-03-08.

Sponsored by Mount Sinai Hospital, Canada · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Mar 2019), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
15
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Bipolar Disorder
  • Major Depressive Disorder

Keywords

  • lithium
  • pharmacokinetics
  • renal
  • kidney
03

In context

Depressive Disorder

4,845 studies on the registry are indexed under Depressive Disorder; 514 are open to participants now.

This study's planned enrollment of 15 is below the median of 80 across 3,999 interventional studies indexed under Depressive Disorder.

Browse Depressive Disorder studies →

Lead sponsor

Mount Sinai Hospital, Canada is the lead sponsor of 157 studies on the registry; 33 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
15 participants (estimated)

Study arms

  • Active comparator
    Once Daily Dosing

    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.

    Diagnostic Test: Lithium level · Diagnostic Test: Serum Creatinine

  • Active comparator
    Twice Daily Dosing

    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.

    Diagnostic Test: Lithium level · Diagnostic Test: Serum Creatinine

Interventions

  • Diagnostic testLithium level

    The level of lithium in the serum

  • Diagnostic testSerum Creatinine

    The level of creatinine (as an indicator of kidney function, to approximate GFR) in the serum

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What researchers measure

Primary outcomes

  1. 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)

    Time frame: once 2 steady state levels have been taken (4-12 days of intervention)

Secondary outcomes

  1. 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

    Time frame: once 2 steady state levels have been taken (4-12 days of intervention) and average creatinine clearance has been calculated

  2. Frequency of selected concurrent medication use

    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

07

Study locations

1 of 1 sites recruiting
  • Mount Sinai Hospital
    Toronto, Ontario M5G 1X5, Canada
    • Virginia Fernandes, PharmD · Contact
    Recruiting
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References and documents

Individual participant data

Plan to share: No — There is no such plan

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 8, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03811860
Lead sponsor
Mount Sinai Hospital, Canada
Responsible party
Virginia Fernandes (Clinical Practice Leader, Psychiatry, Mount Sinai Hospital, Canada) — Principal investigator
First posted
Jan 22, 2019
Start date
Feb 6, 2019
Primary completion
Sep 2019 (estimated)
Completion
Dec 2019 (estimated)
Last update
Mar 8, 2019

Study contacts

Virginia Fernandes, PharmD
Contact
virginia.fernandes@sinaihealthsystem.ca
416-586-4800
Dario A Moscoso, PharmD
Contact
dario.moscoso@sinaihealthsystem.ca
416-586-4800

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2019. You cannot join it, but the record below documents what was studied.

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