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SGLT2-Inhibitors for Sleep Apnea in Heart Failure

Primary Purpose

Heart Failure, Sleep Disordered Breathing

Status
Not yet recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Dapagliflozin
WatchPat
Sponsored by
Columbia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Heart Failure focused on measuring heart failure, sleep disordered breathing, sglt2-inhibitor, sglt2, dapagliflozin, watchpat

Eligibility Criteria

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

Inclusion Criteria:

  • Consent-able adults
  • Diagnosis of heart failure
  • Diagnosis of SDB
  • No contraindication for taking dapagliflozin

Exclusion Criteria:

  • Patients without heart failure
  • Patients without SDB
  • Contraindication for taking dapagliflozin (severe renal impairment, hemodialysis, or history of severe hypoglycemic episodes)

Sites / Locations

  • Vivian and Seymour Milstein Family Heart Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

SGLT2-SDB

Arm Description

Patients with newly diagnosed SDB will be given dapagliflozin (standard dosage, 10mg)

Outcomes

Primary Outcome Measures

Change in Apnea-Hypopnea Index
Change in the apnea-hypopnea index as measured by the WatchPAT device.
Change Berlin Questionnaire Categorization
The Berlin Questionnaire for sleep apnea consists of 3 categories related to the risk of having sleep apnea. Participants are classified as "High Risk" or "Low Risk" for sleep apnea. High risk categorization is assigned when there are 2 or more categories where the score is positive ("positive" defined as a score of 2 or more points). Low risk categorization is assigned when there is 1 or no categories where the score is positive.
Change in Epworth Sleepiness Scale
The Epworth Sleepiness Scale is an 8-item scale measuring sleepiness in various situations. Each situation is scored as 0=no chance of dozing to 3= high chance of dosing. Scores range from 0-24, with a higher score indicating a higher level of sleepiness.

Secondary Outcome Measures

Full Information

First Posted
November 17, 2020
Last Updated
July 31, 2023
Sponsor
Columbia University
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1. Study Identification

Unique Protocol Identification Number
NCT04640493
Brief Title
SGLT2-Inhibitors for Sleep Apnea in Heart Failure
Official Title
The Effect of Sodium Glucose Co-transporter 2 (SGLT2)-Inhibitors on Sleep Disordered Breathing in Heart Failure Patients
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
December 2023 (Anticipated)
Primary Completion Date
August 2025 (Anticipated)
Study Completion Date
August 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Columbia University

4. Oversight

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

5. Study Description

Brief Summary
Heart Failure is a disease involving many different aspects of the human body, including changes in metabolism, the way the body produces and uses energy. Research shows that patients with heart failure often have a sleep disorder called sleep disordered breathing (SDB). It has been shown that SDB is associated with poor outcomes in heart failure patients, but the exact reason is unknown. It is likely that SDB leads to changes in metabolism and hormone status in the body, which is especially dangerous for heart failure patients. There is currently no treatment for SDB in heart failure patients. Recently, with Sodium glucose co-transporter 2 (SGLT2)-Inhibitors a new drug class has been approved for the treatment of advanced heart failure. This drug has effects on the metabolism in heart failure patients, among several other effects. This research project has the aim to investigate if SGLT2 inhibitors can help in the treatment of SDB, as many mechanisms of the drug overlap with the mechanisms how SDB develops. The drug has been approved by the FDA for the treatment of heart failure. The investigators want to study the effect of the drug on SDB by using a home sleep test called Watchpat, which has been approved to diagnose SDB.
Detailed Description
To explore whether SGLT2-Inhibition has a beneficial effect on Sleep Disordered Breathing (SDB) in advanced heart failure patients. This project proposes to carry out research that addresses the established, but in clinical practice under-recognized association between Sleep Disordered Breathing (SDB) and a worse prognosis in patients with heart failure (HF). SDB is highly prevalent in the HF population. Multiple studies have shown that HF accompanied by SDB is associated with an increased mortality compared to the absence of SDB. Two major types of SDB are prevalent in HF: Obstructive Sleep Apnea (OSA) and Central Sleep Apnea (CSA). Mechanistically, it has been proposed that SDB impacts the neurohumoral axis and systemic metabolism and therefore has particularly detrimental effects on the HF patient population. Therapeutic options for the treatment of SDB are limited. Heart Failure is a multisystemic disease leading to maladaptive cardiac and systemic metabolic changes. Recently, with SGLT2-Inhibitors a new drug class has been approved for the treatment of advanced heart failure. This is the first drug class in the HF drug armamentarium targeting cardiometabolic mechanisms. This study seeks to improve the health of individuals with heart failure by exploring whether SGLT2-Inhibition has a beneficial effect on SDB (OSA and CSA) in advanced heart failure patients and therefore may be a novel therapeutic option for the treatment of SDB in advanced HF. The specific aim of this project is to assess the effect of therapy with a SGLT2-I on SDB in ambulatory advanced HF patients by using the WatchPAT-derived apnea-hypopnea index as well as subjective measures of sleep quality using the Berlin Questionnaire and Epworth Sleepiness Scale.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Sleep Disordered Breathing
Keywords
heart failure, sleep disordered breathing, sglt2-inhibitor, sglt2, dapagliflozin, watchpat

7. Study Design

Primary Purpose
Other
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Model Description
Study design is prospective, non-randomized, interventional (non-experimental) pre-post study
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
SGLT2-SDB
Arm Type
Experimental
Arm Description
Patients with newly diagnosed SDB will be given dapagliflozin (standard dosage, 10mg)
Intervention Type
Drug
Intervention Name(s)
Dapagliflozin
Other Intervention Name(s)
FARXIGA
Intervention Description
If patients have been diagnosed with SDB using the WatchPat device, they will start dapagliflozin. Repeat WatchPat SDB assessment will be performed after 3 and 6 months of continuous dapagliflozin therapy.
Intervention Type
Device
Intervention Name(s)
WatchPat
Intervention Description
HF patients undergo SDB testing with the WatchPat device. (non-experimental)
Primary Outcome Measure Information:
Title
Change in Apnea-Hypopnea Index
Description
Change in the apnea-hypopnea index as measured by the WatchPAT device.
Time Frame
6 months
Title
Change Berlin Questionnaire Categorization
Description
The Berlin Questionnaire for sleep apnea consists of 3 categories related to the risk of having sleep apnea. Participants are classified as "High Risk" or "Low Risk" for sleep apnea. High risk categorization is assigned when there are 2 or more categories where the score is positive ("positive" defined as a score of 2 or more points). Low risk categorization is assigned when there is 1 or no categories where the score is positive.
Time Frame
6 months
Title
Change in Epworth Sleepiness Scale
Description
The Epworth Sleepiness Scale is an 8-item scale measuring sleepiness in various situations. Each situation is scored as 0=no chance of dozing to 3= high chance of dosing. Scores range from 0-24, with a higher score indicating a higher level of sleepiness.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Consent-able adults Diagnosis of heart failure Diagnosis of SDB No contraindication for taking dapagliflozin Exclusion Criteria: Patients without heart failure Patients without SDB Contraindication for taking dapagliflozin (severe renal impairment, hemodialysis, or history of severe hypoglycemic episodes)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nir Uriel, MD
Phone
(212) 342-3259
Email
nu2126@cumc.columbia.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nir Uriel, MD
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vivian and Seymour Milstein Family Heart Center
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nir Uriel, MD
First Name & Middle Initial & Last Name & Degree
Nir Uriel, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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SGLT2-Inhibitors for Sleep Apnea in Heart Failure

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