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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02105610
Other study ID # VOLATILE/38/OSR
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date April 14, 2014
Est. completion date September 2018

Study information

Verified date March 2019
Source Università Vita-Salute San Raffaele
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

There is initial evidence that the choice of anesthesia can influence survival in the specific setting of coronary artery bypass grafting surgery (CABG).

A recent international consensus conference included volatile agents among the few drugs/techniques/strategies that might reduce perioperative mortality in cardiac surgery and that should be further studied. Volatile anesthetics (desflurane, isoflurane and sevoflurane) have non-anesthetic pharmacological characteristics that confer cardiac protection when compared to Total IntraVenous Anesthesia (TIVA). Several randomized controlled studies were summarized in a meta-analysis that documented a reduction in perioperative cardiac troponin release and mortality in patients receiving volatile anesthetics when compared to patients receiving a TIVA. There are four published studies (Bignami et al. 2009) (De Hert et al. 2009) (Jackobsen et al. 2007) (Landoni et al. 2007) suggesting that these benefits can translate into a reduced mortality rate in patients receiving volatile agents. The level of evidence for these four studies is not high (one meta-regression, one underpowered randomized controlled study, one retrospective study and one meta-analysis of small randomized studies) and there is need for a large multicentre randomized controlled study to confirm these findings, as suggested by the international consensus conference on this topic published in 2011 (Landoni et al 2011).

The purpose is to provide a large multicentre controlled randomized trial to demonstrate that volatile anesthetics can reduce 1 year mortality from 3% to 2% in patients undergoing CABG (either with or without cardiopulmonary bypass).

The results of this study can support the use of volatile agents in all CABG procedures worldwide (more than 500.000 per year) with 2.500 lives saved per year (in the hypothesis that nowadays half the procedures are performed with a TIVA and that 1 year mortality can be reduced from 3% to 2% using volatile agents).


Recruitment information / eligibility

Status Completed
Enrollment 5400
Est. completion date September 2018
Est. primary completion date October 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- age >18 years

- written informed consent

- scheduled procedures

- planned isolated CABG (multiple bypass are allowed; planned combined intervention such as CABG plus valve surgery are not allowed

Exclusion Criteria:

- pregnancy

- planned valve surgery or surgery on the aorta

- planned locoregional anesthesia without general anesthesia

- unstable or ongoing angina

- recent (< 1 month) or ongoing acute myocardial infarction

- use of sulfonylurea, theophylline or allopurinol

- previous unusual response to an anesthetic agent

- inclusion in other randomised controlled studies in the previous 30 days

- any general anesthesia performed in the previous 30 days

- emergency operation (not scheduled)

- Kidney or liver transplant in medical history

- Liver cirrhosis (Child B or C)

Study Design


Intervention

Drug:
desflurane, isoflurane, sevoflurane

total intravenous anesthetics


Locations

Country Name City State
Bahrain Mohammed Bin Khalifa Bin Sulman Al-Khalifa Cardiac Center - Bahrain Bahrein
Brazil Dante Pazzanese Institute of Cardiology Sao Paulo
Brazil Hospital das Clínicas da Faculdade de Medicina da USP - Istituto do Coracao Sao Paulo Barazil
Bulgaria Heart Center Pontica Burgas
China Beijing Anzhen Hospital, Capital Medical University Beijing
China The Second Xiangya Hospital of Central South University Changsha
China Wuhan Asia Heart Hospital Hubei
China 1st Affiliated Hospital of Fourth Military University Xi'an
Croatia University Hospital Dubrava Dubrava
Czechia General University Hospital, Charles University Prague Czech Republic
Czechia Institute for Clinical and Experimental Medicine Prague Czech Republic
Egypt Mansoura University hospitals Egypt
Egypt Faculty of Medicine - Zagazig University Zagazig
Italy Policlinico San Orsola-Malpighi Bologna
Italy Spedali Civili Brescia
Italy Policlinico Universitario Magna Graecia Catanzaro
Italy Humanitas Milano
Italy Ospedale San Raffaele di Milano, Italy Milano
Italy Azienda Ospedaliera di Padova Padova
Italy Azienda Ospedaliera San Camillo-Forlanini Roma
Italy Policlinico Universitario Campus Biomedico Roma
Italy AOU Città della Salute e della Scienza Torino
Malaysia Hospital Serdang Lumpur
Malaysia University Malaya Medical Centre Lumpur
Malaysia Hospital Pulau Pinang Penang
Malaysia Sarawak General Hospital Sarawak
Portugal Hospital Santa Maria Lisbon
Russian Federation Federal Centre for Cardiac Surgery Astrakhan
Russian Federation Ural Institute of Cardiology Ekaterinburg
Russian Federation Scientific Research Institute for Complex Issues of Cardiovascular Disease Kemerovo
Russian Federation Moscow Clinical Regional Research Institute Moscow
Russian Federation Negovskiy Reanimatology Research Institute Moscow
Russian Federation State Research Institute of Circulation Pathology Novosibirsk
Russian Federation Federal Almazov Medical Research Centre Saint Petersburg
Saudi Arabia King Abdullah Medical City - KAMC Mecca
Serbia Institute of Cardiovascular Diseases "Dedinje" Belgrade

Sponsors (1)

Lead Sponsor Collaborator
Università Vita-Salute San Raffaele

Countries where clinical trial is conducted

Bahrain,  Brazil,  Bulgaria,  China,  Croatia,  Czechia,  Egypt,  Italy,  Malaysia,  Portugal,  Russian Federation,  Saudi Arabia,  Serbia, 

References & Publications (3)

Landoni G, Greco T, Biondi-Zoccai G, Nigro Neto C, Febres D, Pintaudi M, Pasin L, Cabrini L, Finco G, Zangrillo A. Anaesthetic drugs and survival: a Bayesian network meta-analysis of randomized trials in cardiac surgery. Br J Anaesth. 2013 Dec;111(6):886-96. doi: 10.1093/bja/aet231. Epub 2013 Jul 12. — View Citation

Landoni G, Lomivorotov V, Pisano A, Nigro Neto C, Benedetto U, Biondi Zoccai G, Gemma M, Frassoni S, Agrò FE, Baiocchi M, Barbosa Gomes Galas FR, Bautin A, Bradic N, Carollo C, Crescenzi G, Elnakera AM, El-Tahan MR, Fominskiy E, Farag AG, Gazivoda G, Gianni S, Grigoryev E, Guarracino F, Hanafi S, Huang W, Kunst G, Kunstyr J, Lei C, Lembo R, Li ZJ, Likhvantsev V, Lozovskiy A, Ma J, Monaco F, Navalesi P, Nazar B, Pasyuga V, Porteri E, Royse C, Ruggeri L, Riha H, Santos Silva F, Severi L, Shmyrev V, Uvaliev N, Wang CB, Wang CY, Winterton D, Yong CY, Yu J, Bellomo R, Zangrillo A. MortalitY in caRdIAc surgery (MYRIAD): A randomizeD controlled trial of volatile anesthetics. Rationale and design. Contemp Clin Trials. 2017 Aug;59:38-43. doi: 10.1016/j.cct.2017.05.011. Epub 2017 May 19. — View Citation

Landoni G, Rodseth RN, Santini F, Ponschab M, Ruggeri L, Székely A, Pasero D, Augoustides JG, Del Sarto PA, Krzych LJ, Corcione A, Slullitel A, Cabrini L, Le Manach Y, Almeida RM, Bignami E, Biondi-Zoccai G, Bove T, Caramelli F, Cariello C, Carpanese A, Clarizia L, Comis M, Conte M, Covello RD, De Santis V, Feltracco P, Giordano G, Pittarello D, Gottin L, Guarracino F, Morelli A, Musu M, Pala G, Pasin L, Pezzoli I, Paternoster G, Remedi R, Roasio A, Zucchetti M, Petrini F, Finco G, Ranieri M, Zangrillo A. Randomized evidence for reduction of perioperative mortality. J Cardiothorac Vasc Anesth. 2012 Oct;26(5):764-72. doi: 10.1053/j.jvca.2012.04.018. Epub 2012 Jun 20. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary mortality 1 year
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