The Routine Use of SSRI's at the Initiation of End-stage Renal Disease Treatment (RoSIE)

End Stage Renal Disease Clinical Trial

— RoSIE  

Official title:

A Pilot Study to Evaluate the Feasibility and Safety of Performing a Double Blind, Placebo-controlled, Randomized Controlled Trial of the Routine Use of SSRI's at the Initiation of End-stage Renal Disease Treatment

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02407821
• Other study ID #: 01
• Status: Terminated
• Phase: Phase 2
• Start date: March 2015
• Est. completion date: January 2017

Study information

• Verified date: September 2018
• Source: University Health Network, Toronto
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In this study the investigators hypothesize that antidepressant therapy may improve the overall welling of patients with acute or chronic kidney disease when given around the time of starting chronic dialysis therapy. This study is a pilot, randomized controlled trial that aims to examine whether prescribing oral escitalopram to all incident dialysis patients is safe and feasible.

Description:

Over 120,000 people with kidney disease start chronic dialysis therapy across North America each year. In addition to high mortality, studies uniformly report high rates of depression, pain and non-specific symptoms after dialysis is started. Suicide rates are high, particularly early in the treatment history, and withdrawal from dialysis is increasingly common in recent years, suggesting a high burden of depressive symptoms. While various treatments appear to be effective, there are multiple barriers preventing patients from getting or accepting appropriate care for depression. The investigators hypothesize that antidepressant therapy may improve morbidity and mortality when prescribed to patients with acute or chronic kidney disease (CKD) around the time of starting chronic dialysis therapy.

This is a phase II, multi-centre, double blind, randomized controlled trial to compare the safety and feasibility of oral escitalopram to placebo in incident dialysis patients. Those who have started chronic dialysis therapy within 12 weeks of being identified will be eligible for the study. Participants will randomized 1:1 to receive either escitalopram or placebo daily for 26 weeks.

The primary outcome is feasibility in terms of recruitment rates and protocol compliance. The secondary outcomes include estimates of safety (adverse events) and efficacy (hospitalization days, mortality, and changes in depression and quality of life scores). This pilot trial is intended to guide and inform the design of a full scale study to evaluate whether the routine use of escitalopram can improve the quality of life and hospital free days in patients on dialysis, as compared to placebo.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 25
• Est. completion date: January 2017
• Est. primary completion date: January 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 25 Years and older

Eligibility

Inclusion Criteria:

1. Male or Female aged = 25 years

2. Patient or substitute decision maker willing and able to give informed consent

3. Incident to dialysis defined as within a 12-week window from the first dialysis treatment (1 week prior to, to 11 weeks after). Patients on all forms of dialysis except CRRT (including peritoneal dialysis, home hemodialysis, in-centre intermittent hemodialysis and nocturnal dialysis) will be eligible. Patients returning to dialysis after transplant graft loss will be eligible.

Exclusion Criteria:

1. Past history of allergy to, or intolerance of, escitalopram

2. Known severe hepatic dysfunction

3. Recent history of active bleeding within the past 3 months (e.g. gastrointestinal bleeding requiring hospitalization) or known bleeding disorder

4. Current use of class I anti-arrhythmic medications; SSRI or SNRI antidepressants; pimozide, MAO inhibitors, reserpine, guanethidine, cimetidine or methyldopa, omeprazole; tri-cyclic and tetra-cyclic anti-depressants, neuroleptics or anti-convulsants, triptans, tramadol, linezolid, tryptophan, and St. John's Wort; but not gabapentin

5. Past treatment failure for depression with escitalopram or with = 2 antidepressant treatments of at least 6 weeks duration each

6. Initiation of psychotherapy for depression in the 3 months prior to study entry

7. Alcohol or substance abuse or dependence that requires acute detoxification at study entry

8. Present or past psychosis or bipolar disorder, schizophrenia or any other psychotic disorder documented in medical records

9. Suicidal ideation defined as the patient is at significant risk of suicide on the Columbia Suicide Scale71 or has attempted suicide within 6 months prior to the Screening Visit

10. Clinically-identified major depressive disorder that, in the opinion of the clinical team, requires treatment

11. Pregnancy, lactation and women of childbearing potential not using adequate contraception

12. Abnormal QTc at baseline: QTcF interval >600 ms (based on the Fredericia correction where QTcF = QT/RR0.33)66

13. Lactose intolerance (as placebo contains lactose)

14. Known uncontrolled glaucoma

15. Patients requiring treatment with continuous renal replacement therapy (CRRT)

16. Documented history of brain tumour

Related Conditions & MeSH terms

• End Stage Renal Disease
• Kidney Diseases
• Kidney Failure, Chronic

Intervention

Drug:
• Escitalopram
Dose will be initiated at 5 mg daily. At two weeks, a safety and tolerability assessment will be performed, and if tolerated, the dose will be increased to 10 mg daily. At 24 weeks, the medication will be titrated downwards to 5 mg daily for a further two weeks before discontinuation.
• Placebo
The matching placebo will be up-titrated and down-titrated at the same time intervals as the active medication.

Locations

Country	Name	City	State
Canada	St. Joseph's Healthcare Hamilton	Hamilton	Ontario
Canada	St. Michael's Hospital	Toronto	Ontario
Canada	University Health Network	Toronto	Ontario

Sponsors (4)

Lead Sponsor	Collaborator
University Health Network, Toronto	McMaster University, St. Michael's Hospital, Toronto, University of Toronto

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion of consecutive incident dialysis patients that are eligible		12 months
Primary	Proportion of eligible patients that will consent to randomization		12 months
Primary	Proportion of randomized patients that comply with their group assignment	Compliance defined as >80% of doses taken	12 months
Secondary	Serious adverse events		12 months
Secondary	Number of patients withdrawn from the study drug due to QTc prolongation		12 months
Secondary	Completion rate for all secondary outcome measures (KDQoL, HUI-III, PHQ-9, Handgrip and 2-Minute Walk Test)		3 months and 6 months
Secondary	Death		12 months
Secondary	Hospital-free days		12 months