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Iv Amiodarone Versus Iv Procainamide to Treat Haemodynamically Well Tolerated Ventricular Tachycardia

Primary Purpose

Ventricular Tachycardia, Wide QRS Tachycardia

Status
Terminated
Phase
Phase 4
Locations
Spain
Study Type
Interventional
Intervention
iv Amiodarone
iv Procainamide
Sponsored by
Hospital General Universitario Gregorio Marañon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ventricular Tachycardia focused on measuring Ventricular tachycardia

Eligibility Criteria

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

Inclusion Criteria:

  • Patients with stable tachycardia ≥120 lpm, QRS ≥120 ms and haemodynamically well tolerated defined as: 1)Systolic blood pressure ≥90 mmHg, 2) absence of dyspnea at rest, 3)absence of peripheric hypoperfusion signs and 4)no severe angina.
  • Age > 18 years
  • Written inform consent obtained

Exclusion Criteria:

  • Treatment with iv amiodarone or iv procainamide during the previous 24 hours
  • QRS tachycardia <120 ms
  • Patients with QRS ≥120 ms tachycardia with haemodynamic compromise that requires urgent cardioversion for termination
  • Irregular tachycardia
  • Tachycardia that is considered as supraventricular due to physician criteria (adenosine and/or vagal manoeuvres response)
  • Patient that do not want to cooperate

Sites / Locations

  • Hospital El Escorial
  • Hospital Universitario de Getafe
  • Hospital Santa María del Rosell
  • Fundación Hospitalaria de Cieza
  • Hospital Los Arcos
  • Hospital General
  • Hospital Clinic
  • Hospital Vall d'Hebron
  • Hospital de Basurto
  • Hospital San Cecilio
  • Hospital Virgen de las Nieves
  • Hospital General Universitario Gregorio Marañón
  • Hospital 12 de Octubre
  • Hospital Clínico San Carlos
  • Hospital de La Princesa
  • Hospital de Móstoles
  • Hospital General Universitario La Paz
  • Hospital Puerta de Hierro
  • Hospital Carlos Haya
  • Hospital Virgen de la Arrixaca
  • Hospital Clínico Virgen de la Victoria
  • Hospital de Son Dureta
  • Hospital de Son Llatzer
  • Hospital de Donostia
  • Hospital de Valme
  • Hospital Universitario Virgen del Rocío
  • Hospital Virgen de la Salud
  • Hopital Clínico Universitario
  • Hospital Río Hortega

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Group 1

Group 2

Arm Description

IV procainamide (single dose: 10 mg/kg over 20 min)

IV Amiodarone (single dose: 5 mg/kg over 20 min)

Outcomes

Primary Outcome Measures

To compare clinically significant cardiac adverse events occurring within 40 minutes from treatment initiation

Secondary Outcome Measures

To compare efficacy of both therapies in relation to episode termination
To compare the rate of total adverse events, cardiac and non cardiac, occurring during an observation period of 24 hours after treatment was applied

Full Information

First Posted
October 3, 2006
Last Updated
April 4, 2016
Sponsor
Hospital General Universitario Gregorio Marañon
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1. Study Identification

Unique Protocol Identification Number
NCT00383799
Brief Title
Iv Amiodarone Versus Iv Procainamide to Treat Haemodynamically Well Tolerated Ventricular Tachycardia
Official Title
Comparison of Intravenous Amiodarone Versus Intravenous Procainamide for the Acute Treatment of Regular and Haemodynamically Well Tolerated Wide QRS Tachycardia (Probably of Ventricular Origen). The PROCAMIO Multicenter Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Terminated
Why Stopped
Steering Committee decision after inclusion of 74 patients after 6 years and very slow inclusion rate
Study Start Date
September 2005 (undefined)
Primary Completion Date
June 2011 (Actual)
Study Completion Date
June 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital General Universitario Gregorio Marañon

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether intravenous amiodarone has less cardiac significant adverse events compared to intravenous procainamide in the acute treatment of haemodynamically well tolerated wide QRS tachycardia, the majority of them of probably ventricular origen.
Detailed Description
Multicenter, prospective and randomized study in phase IV. A total of 302 patients will be included in the study within 40-50 institutions in Spain. Patients with regular and monomorphic tachycardia ≥ 120 bpm, QRS ≥ 120 ms and haemodynamically well tolerated will be randomized to receive iv amiodarone (single dosage: 5 mg/kg in 20 minutes) vs iv procainamide (single dosage: 10 mg/kg in 20 minutes). The study period will be 40 minutes from infusion initiation. Study variables include the presence of clinically cardiac significant adverse events: hypotension, syncope, heart failure, symptomatic sinus bradycardia, AV block, proarrhythmia and tachycardia acceleration (<20 lpm)and death. Total observation period will be 24 hours after the end of the infusion.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ventricular Tachycardia, Wide QRS Tachycardia
Keywords
Ventricular tachycardia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
302 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group 1
Arm Type
Active Comparator
Arm Description
IV procainamide (single dose: 10 mg/kg over 20 min)
Arm Title
Group 2
Arm Type
Active Comparator
Arm Description
IV Amiodarone (single dose: 5 mg/kg over 20 min)
Intervention Type
Drug
Intervention Name(s)
iv Amiodarone
Intervention Type
Drug
Intervention Name(s)
iv Procainamide
Primary Outcome Measure Information:
Title
To compare clinically significant cardiac adverse events occurring within 40 minutes from treatment initiation
Time Frame
40 minutes
Secondary Outcome Measure Information:
Title
To compare efficacy of both therapies in relation to episode termination
Time Frame
40 minuutes
Title
To compare the rate of total adverse events, cardiac and non cardiac, occurring during an observation period of 24 hours after treatment was applied
Time Frame
24 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with stable tachycardia ≥120 lpm, QRS ≥120 ms and haemodynamically well tolerated defined as: 1)Systolic blood pressure ≥90 mmHg, 2) absence of dyspnea at rest, 3)absence of peripheric hypoperfusion signs and 4)no severe angina. Age > 18 years Written inform consent obtained Exclusion Criteria: Treatment with iv amiodarone or iv procainamide during the previous 24 hours QRS tachycardia <120 ms Patients with QRS ≥120 ms tachycardia with haemodynamic compromise that requires urgent cardioversion for termination Irregular tachycardia Tachycardia that is considered as supraventricular due to physician criteria (adenosine and/or vagal manoeuvres response) Patient that do not want to cooperate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jesús Almendral, MD
Organizational Affiliation
Hospital General Universitario Gregorio Marañón. Madrid. Spain
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Fernando Arribas, MD
Organizational Affiliation
Hospital General Universitario 12 de Octubre. Madrid. Spain
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Rafael Peinado, MD
Organizational Affiliation
Hospital General Universitario La Paz. Madrid. Spain
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Alfonso Martín, MD
Organizational Affiliation
Hospital de Móstoles. Madrid. Spain
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Carmen del Arco, MD
Organizational Affiliation
Hospital de la Princesa. Madrid. Spain
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Dolores Vigil, MD
Organizational Affiliation
Hospital general Universitario Gregorio Marañón. Madrid. Spain
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Mercedes Ortiz, PhD
Organizational Affiliation
Hospital General Universitario Gregorio Marañón. Madrid. Spain
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Blanca Coll-Vinent, MD
Organizational Affiliation
Hospital Clinic. Barcelona. Spain
Official's Role
Study Director
Facility Information:
Facility Name
Hospital El Escorial
City
El Escorial
State/Province
Madrid
Country
Spain
Facility Name
Hospital Universitario de Getafe
City
Getafe
State/Province
Madrid
Country
Spain
Facility Name
Hospital Santa María del Rosell
City
Cartagena
State/Province
Murcia
Country
Spain
Facility Name
Fundación Hospitalaria de Cieza
City
Cieza
State/Province
Murcia
Country
Spain
Facility Name
Hospital Los Arcos
City
San Javier
State/Province
Murcia
Country
Spain
Facility Name
Hospital General
City
Alicante
Country
Spain
Facility Name
Hospital Clinic
City
Barcelona
Country
Spain
Facility Name
Hospital Vall d'Hebron
City
Barcelona
Country
Spain
Facility Name
Hospital de Basurto
City
Bilbao
Country
Spain
Facility Name
Hospital San Cecilio
City
Granada
Country
Spain
Facility Name
Hospital Virgen de las Nieves
City
Granada
Country
Spain
Facility Name
Hospital General Universitario Gregorio Marañón
City
Madrid
ZIP/Postal Code
28007
Country
Spain
Facility Name
Hospital 12 de Octubre
City
Madrid
Country
Spain
Facility Name
Hospital Clínico San Carlos
City
Madrid
Country
Spain
Facility Name
Hospital de La Princesa
City
Madrid
Country
Spain
Facility Name
Hospital de Móstoles
City
Madrid
Country
Spain
Facility Name
Hospital General Universitario La Paz
City
Madrid
Country
Spain
Facility Name
Hospital Puerta de Hierro
City
Madrid
Country
Spain
Facility Name
Hospital Carlos Haya
City
Malaga
Country
Spain
Facility Name
Hospital Virgen de la Arrixaca
City
Murcia
Country
Spain
Facility Name
Hospital Clínico Virgen de la Victoria
City
Málaga
Country
Spain
Facility Name
Hospital de Son Dureta
City
Palma de Mallorca
Country
Spain
Facility Name
Hospital de Son Llatzer
City
Palma de Mallorca
Country
Spain
Facility Name
Hospital de Donostia
City
San Sebastián
Country
Spain
Facility Name
Hospital de Valme
City
Sevilla
Country
Spain
Facility Name
Hospital Universitario Virgen del Rocío
City
Sevilla
Country
Spain
Facility Name
Hospital Virgen de la Salud
City
Toledo
Country
Spain
Facility Name
Hopital Clínico Universitario
City
Valencia
Country
Spain
Facility Name
Hospital Río Hortega
City
Valladolid
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
10966669
Citation
Guidelines 2000 for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Part 6: advanced cardiovascular life support: section 5: pharmacology I: agents for arrhythmias. The American Heart Association in collaboration with the International Liaison Committee on Resuscitation. Circulation. 2000 Aug 22;102(8 Suppl):I112-28. No abstract available.
Results Reference
background
PubMed Identifier
16314375
Citation
ECC Committee, Subcommittees and Task Forces of the American Heart Association. 2005 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Circulation. 2005 Dec 13;112(24 Suppl):IV1-203. doi: 10.1161/CIRCULATIONAHA.105.166550. Epub 2005 Nov 28. No abstract available.
Results Reference
background
PubMed Identifier
16935995
Citation
Zipes DP, Camm AJ, Borggrefe M, Buxton AE, Chaitman B, Fromer M, Gregoratos G, Klein G, Moss AJ, Myerburg RJ, Priori SG, Quinones MA, Roden DM, Silka MJ, Tracy C, Smith SC Jr, Jacobs AK, Adams CD, Antman EM, Anderson JL, Hunt SA, Halperin JL, Nishimura R, Ornato JP, Page RL, Riegel B, Blanc JJ, Budaj A, Dean V, Deckers JW, Despres C, Dickstein K, Lekakis J, McGregor K, Metra M, Morais J, Osterspey A, Tamargo JL, Zamorano JL; American College of Cardiology/American Heart Association Task Force; European Society of Cardiology Committee for Practice Guidelines; European Heart Rhythm Association; Heart Rhythm Society. ACC/AHA/ESC 2006 Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death: a report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiology Committee for Practice Guidelines (writing committee to develop Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death): developed in collaboration with the European Heart Rhythm Association and the Heart Rhythm Society. Circulation. 2006 Sep 5;114(10):e385-484. doi: 10.1161/CIRCULATIONAHA.106.178233. Epub 2006 Aug 25. No abstract available.
Results Reference
background
Links:
URL
https://operation.kikamedical.com/procamio
Description
Protocol home's page

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Iv Amiodarone Versus Iv Procainamide to Treat Haemodynamically Well Tolerated Ventricular Tachycardia

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