NCT01186783

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

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
70

participants targeted

Target at P50-P75 for phase_2

Timeline
Completed

Started May 2010

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2010

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

August 17, 2010

Completed
6 days until next milestone

First Posted

Study publicly available on registry

August 23, 2010

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2011

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2012

Completed
Last Updated

September 8, 2010

Status Verified

September 1, 2010

Enrollment Period

1.5 years

First QC Date

August 17, 2010

Last Update Submit

September 7, 2010

Conditions

Keywords

heart ratemultiple organ dysfunction syndromeivabradinesepsiscardiogenic shock

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 INTERVENTION

All patients receive established medical therapy according to current guidelines and therapeutic standards.

ivabradine (add-on)

ACTIVE COMPARATOR

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.

Drug: ivabradine

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

Also known as: Procoralan
ivabradine (add-on)

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

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

RECRUITING

Related Publications (36)

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    PMID: 18651035BACKGROUND
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  • Nuding S, Ebelt H, Hoke RS, Krummenerl A, Wienke A, Muller-Werdan U, Werdan K. Reducing elevated heart rate in patients with multiple organ dysfunction syndrome by the I (f) (funny channel current) inhibitor ivabradine : MODI (f)Y trial. Clin Res Cardiol. 2011 Oct;100(10):915-23. doi: 10.1007/s00392-011-0323-2. Epub 2011 Jun 3.

MeSH Terms

Conditions

Multiple Organ FailureSepsisShock, Cardiogenic

Interventions

Ivabradine

Condition Hierarchy (Ancestors)

ShockPathologic ProcessesPathological Conditions, Signs and SymptomsInfectionsSystemic Inflammatory Response SyndromeInflammationMyocardial InfarctionMyocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular DiseasesInfarctionIschemiaNecrosis

Intervention Hierarchy (Ancestors)

BenzazepinesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-RingHeterocyclic Compounds

Study Officials

  • Karl Werdan, MD, Professor

    Medical Faculty of the Martin-Luther-University Halle-Wittenberg, Germany

    STUDY CHAIR
  • 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

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Karl Werdan, MD, Professor

CONTACT

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

Locations