Reducing Elevated Heart Rate in Patients With Multiple Organ Dysfunction Syndrome (MODS) by Ivabradine
MODIfY
1 other identifier
interventional
70
1 country
1
Brief Summary
MODIfY is a prospective, single center, open label, randomized, controlled two arms, Phase II-trial to evaluate the ability of ivabradine to reduce an elevated heart rate in Multiple Organ Dysfunction Syndrome (MODS) patients. The primary end point is the proportion of patients with a reduction of heart rate by at least 10 beats per minute (bpm) within 4 days. This trial will randomize 70 patients (men and women, aged ≥ 18 years) with newly diagnosed MODS (Acute Physiology and Chronic Health Evaluation (APACHE) II-score ≥ 20, diagnosis within ≤ 24 hours), with an elevated heart rate (sinus rhythm with HR ≥ 90 bpm) and contraindications to beta-blockers (BBs). Treatment period will last 4 days. All patients will be followed for up to six months.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_2
Started May 2010
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2010
CompletedFirst Submitted
Initial submission to the registry
August 17, 2010
CompletedFirst Posted
Study publicly available on registry
August 23, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2012
CompletedSeptember 8, 2010
September 1, 2010
1.5 years
August 17, 2010
September 7, 2010
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
mean heart rate
percenage of patients with a reduction of the mean heart rate of at least 10 bpm 96 hours after the start of trial treatment
4 days
Secondary Outcomes (13)
morbidity
4 days
hemodynamic parameters
4 days
catecholamine dosage
4 days
microcirculation
4 days
endothelial function
4 days
- +8 more secondary outcomes
Study Arms (2)
standard treatment
NO INTERVENTIONAll patients receive established medical therapy according to current guidelines and therapeutic standards.
ivabradine (add-on)
ACTIVE COMPARATORPatients in the ivabradine treatment arm receive an additional enteral preparation (orally, via nasogastric tube or percutaneous endoscopic gastrostomy-probe) of ivabradine for 4 days.
Interventions
Patients in the ivabradine treatment arm receive an additional enteral preparation (orally, via nasogastric tube or percutaneous endoscopic gastrostomy-probe) of ivabradine for 4 days. Day 1 and 2: 5,0 mg ivabradine b.i.d. if heart rate ≥60bpm (acute renal failure: ≥70bpm) Day 3 and 4: 5,0 mg ivabradine b.i.d. if 60bpm≥heart rate\<90bpm (acute renal failure: 70bpm≥heart rate \<90bpm 7,5 mg ivabradine b.i.d. if heart rate ≥90bpm
Eligibility Criteria
You may qualify if:
- Multiple organ dysfunction syndrome (APACHE II score ≥ 20) due to coronary and non-coronary etiology
- Multiple organ dysfunction syndrome diagnosed ≤ 24 h
- Sinus rhythm with heart rate ≥ 90bpm
- Existing contraindications to beta-receptor blockade
- Written informed consent or identified or suspected positive will with respect to the trial treatment
You may not qualify if:
- Patients who have not yet completed the 18th year of age
- Pregnancy, lactation
- Patients with a history of pre-existing chronic renal failure with a glomerular filtration rate \<30ml/min
- Patients with malignant hyperthermia
- Burn patients
- Patients with acute rejection after organ transplantation
- Patients with bleedings and need for transfusion
- Resuscitated patients with suspected hypoxic brain injury
- Patients who have participated or participate in other studies within the last 3 months
- Other types of shock than septic or cardiogenic shock
- Patients with severe valvular heart disease
- Hypersensitivity to the active substance or any of the excipients
- Severe hepatic insufficiency
- Sick sinus syndrome
- Sinu-atrial block
- +3 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Martin-Luther-Universität Halle-Wittenberglead
- Serviercollaborator
- KKS Netzwerkcollaborator
Study Sites (1)
Department of Medicine III of the University Clinics Halle (Saale) of the Martin-Luther-University Halle-Wittenberg
Halle, Saxony-Anhalt, 06120, Germany
Related Publications (36)
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PMID: 21638157DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Karl Werdan, MD, Professor
Medical Faculty of the Martin-Luther-University Halle-Wittenberg, Germany
- PRINCIPAL INVESTIGATOR
Henning Ebelt, MD
Medical Faculty of the Martin-Luther-University Halle-Wittenberg, Germany
- PRINCIPAL INVESTIGATOR
Sebastian Nuding, MD
Medical Faculty of the Martin-Luther-University Halle-Wittenberg, Germany
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
August 17, 2010
First Posted
August 23, 2010
Study Start
May 1, 2010
Primary Completion
November 1, 2011
Study Completion
May 1, 2012
Last Updated
September 8, 2010
Record last verified: 2010-09