Trial Outcomes & Findings for The Hemodynamic Effects of SGLT2i in Acute Decompensated Heart Failure (NCT NCT05346653)

NCT ID: NCT05346653

Last Updated: 2024-09-04

Results Overview

Measured by pulmonary artery catheter

Recruitment status

TERMINATED

Study phase

PHASE4

Target enrollment

1 participants

Primary outcome timeframe

4 days

Results posted on

2024-09-04

Participant Flow

Participant milestones

Participant milestones
Measure
SGLT2i
Participants will be treated with a SGLT2i during their ICU stay. The SGLT2i and heart failure care will be managed according to routine care, and data will be collected from the participant's medical record. SGLT2i: dapagliflozin (10 mg daily)
No SGLT2i
Participants will not be treated with a SGLT2i during their ICU stay. Heart failure care will be managed according to routine care, and data will be collected from the participant's medical record. No SGLT2i: No SGLT2i
Overall Study
STARTED
0
0
Overall Study
COMPLETED
0
0
Overall Study
NOT COMPLETED
0
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

The Hemodynamic Effects of SGLT2i in Acute Decompensated Heart Failure

Baseline characteristics by cohort

Baseline data not reported

PRIMARY outcome

Timeframe: 4 days

Population: Only 1 subject consented to the study and was not eligible for randomization.

Measured by pulmonary artery catheter

Outcome measures

Outcome data not reported

PRIMARY outcome

Timeframe: 4 days

Population: Only 1 subject consented to the study and was not eligible for randomization.

Measured by pulmonary artery catheter

Outcome measures

Outcome data not reported

Adverse Events

SGLT2i

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

No SGLT2i

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Sr. Compliance Specialist

University of Chicago

Phone: 773-702-6505

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place