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Semaglutide

Ozempic, Rybelsus, Wegovy

Quick Stats
Studies 78
Trials 100
Withdrawn PHASE3 INTERVENTIONAL NCT04885634

Semaglutide for the Reduction of Arrhythmia Burden in Overweight AF Patients

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

The purpose of this pilot study is to assess the feasibility of a double-blind, randomized placebo-controlled trial of semaglutide 2.4 mg subcutaneously once weekly on top of standard care compared to standard care alone.

Detailed Description

The SOCRATES-AF pilot study is a prospective, parallel-group, double-blind, randomized controlled trial in patients with paroxysmal or early persistent atrial fibrillation and overweight and obesity. The primary objective is to assess the feasibility of a double-blind, randomized placebo-controlled trial of semaglutide 2.4 mg subcutaneously (s.c.) once weekly on top of current standard care (lifestyle and risk factor management, oral anticoagulant and rate control therapy) versus current standard care alone in overweight or obese patients with symptomatic paroxysmal or early persistent AF. To assess recurrences of atrial fibrillation all participants will receive an implantable cardiac monitor.

Interventions

Name: Semaglutide Injectable Product
Type: DRUG
Description: Subcutaneous injection of Semaglutide 2.4 mg once weekly
Name: Placebo
Type: DRUG
Description: Subcutaneous injection of volume-matched placebo once weekly

Primary Outcomes

Measure: Number of Participants to Complete Recruitment
TimeFrame: Up to 68 weeks, until end of treatment
Description: Recruit 100 patients at an average recruitment rate of 2 patients per centre per month
Measure: Number of Participants to Complete Follow-up
TimeFrame: Up to 75 weeks, until final follow-up
Description: Achieve complete follow-up on 90% or more of patients
Measure: Total Resource Requirement
TimeFrame: Up to 75 weeks, until final follow-up
Description: Determine the resource requirements, i.e. primarily time spent per included patient, to achieve the recruitment and follow-up goals

Trial Information

NCT ID

NCT04885634

Status

Withdrawn

Study Type

INTERVENTIONAL

Phases

PHASE3

Sponsor

Axel Brandes

Last Updated

December 15, 2025