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Efficacy and Safety of Dexmedetomidine in the Analgesic Prophylaxis , in Patients Undergoing Cardiovascular Surgery

Primary Purpose

Cardiopathy, Coronary Artery Disease, Valve Heart Disease

Status
Unknown status
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Dexmedetomidine
0,9% Saline
Sponsored by
University of Sao Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cardiopathy focused on measuring Dexmedetomidine, Cardiac surgery, Analgesia

Eligibility Criteria

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

Inclusion Criteria:

  • Patients at least 18 years old and who are undergoing cardiac procedures (coronary artery bypass, valve replacement or combined procedure), with cardiopulmonary by- pass.

Exclusion Criteria:

  • Congenital heart disease
  • Infective endocarditis
  • Acute myocardial infarction (<two weeks)
  • Pregnancy
  • Cancer
  • Left ventricle ejection fraction < 40%
  • Cardiogenic shock
  • Emergent procedure
  • Use of vasopressor and/or inotrope, in the preoperative
  • Liver disfunction
  • Renal replacement therapy
  • Nephrectomy
  • Previous renal transplantation
  • Patients who are participating in another clinical research

Sites / Locations

  • Nova Esperança University HospitalRecruiting
  • Heart Institute (InCor), Univ. of Sao Paulo Medical SchoolRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Group Dexmedetomidine

Group 0,9% Saline

Arm Description

The patient will receive Dexmedetomidine, at the rate of 0,3μg/ kg/h, in continuous intravenous infusion from the initiation of the anesthesia up to the end of the procedure, except during the cardiopulmonary by-pass.

The patient will receive a 0,9% saline, in continuous intravenous infusion, from the initiation of the anesthesia up to the end of the procedure, except during the cardiopulmonary by-pass.

Outcomes

Primary Outcome Measures

Pain 24 hours after cardiac surgery.
The assessment of pain intensity, in patients with self- reporting, will be done by: Numeric Rating Scale (NRS) 0- 10. Possible score range from 0 (no pain) to 10 (worst pain ever ). The assessment of pain intensity, in patients on mechanical ventilation, will be done by: Behavioral Pain Scale, through facial expression (score 1-4), upper limb movement (score 1-5) and compliance with mechanical ventilation (score 1-3). Possible score range from 3 (no pain) to 12 (maximum pain).

Secondary Outcome Measures

Opioid consumption.
Opioid used for the pain control. This will be noted in the medical record.

Full Information

First Posted
October 3, 2021
Last Updated
October 14, 2021
Sponsor
University of Sao Paulo
Collaborators
Federal University of Paraíba
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1. Study Identification

Unique Protocol Identification Number
NCT05079672
Brief Title
Efficacy and Safety of Dexmedetomidine in the Analgesic Prophylaxis , in Patients Undergoing Cardiovascular Surgery
Official Title
Efficacy and Safety of Dexmedetomidine in the Analgesic Prophylaxis , in Patients Undergoing Cardiovascular Surgery: Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
October 7, 2021 (Actual)
Primary Completion Date
October 10, 2022 (Anticipated)
Study Completion Date
October 10, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo
Collaborators
Federal University of Paraíba

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
Acute pain is one of the complications after cardiothoracic surgeries . It can delay patients´recovery and may increase patients´morbity and mortality. This study intends to evaluate Dexmedetomidine, a highly selective α- 2 receptor agonist, that is currently applied safely and efficiently in intraoperative cardiac surgery. It has analgesic, sedative, anxiolytic and sympatholytic properties, without respiratory- depressant effect. The aim of this study is to investigate whether the intraoperative use of dexmedetomidine is better than the standard analgesia used in the intraoperative period to reduce pain and the consequences of it.
Detailed Description
This project is a prospective, double-blinded and randomized clinical trial. Eligible participants are assigned in a 1:1 ratio to either the intervention group (Group Dexmedetomidine) or control group (Group Saline 0,9%), after written informed consent to be obtained. The patients will undergo elective cardiac surgery, with extracorporeal circulation. In the operating room, patients will be monitored for pulse oximetry, invasive blood pressure, electrocardiograms, capnography, central venous pressure and nasopharyngeal temperature probe. Induction of anesthesia is performed with intravenous midazolam, fentanyl, etomidate and neuromuscular blocking agent. Anesthesia is maintained with sevoflurane. Dexmedetomidine, at the rate of 0,3μg/ kg/h, or placebo will be infused from the initiation of the anesthesia up to the end of the procedure, except during the cardiopulmonary by-pass. Placebo is a 0,9% saline. The follow up of the assessment of the groups will extend to the postoperative ICU, where data will be collected, during the first 24 hours after surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiopathy, Coronary Artery Disease, Valve Heart Disease, Pain
Keywords
Dexmedetomidine, Cardiac surgery, Analgesia

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
102 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group Dexmedetomidine
Arm Type
Active Comparator
Arm Description
The patient will receive Dexmedetomidine, at the rate of 0,3μg/ kg/h, in continuous intravenous infusion from the initiation of the anesthesia up to the end of the procedure, except during the cardiopulmonary by-pass.
Arm Title
Group 0,9% Saline
Arm Type
Placebo Comparator
Arm Description
The patient will receive a 0,9% saline, in continuous intravenous infusion, from the initiation of the anesthesia up to the end of the procedure, except during the cardiopulmonary by-pass.
Intervention Type
Drug
Intervention Name(s)
Dexmedetomidine
Intervention Description
Dexmedetomidine injectable solution, at the rate of 0,3μg/ kg/h, will be infused from the initiation of the anesthesia up to the end of the procedure, except during the cardiopulmonary by-pass.
Intervention Type
Drug
Intervention Name(s)
0,9% Saline
Intervention Description
Saline 0,9% will be infused from the initiation of the anesthesia up to the end of the procedure, except during the cardiopulmonary by- pass.
Primary Outcome Measure Information:
Title
Pain 24 hours after cardiac surgery.
Description
The assessment of pain intensity, in patients with self- reporting, will be done by: Numeric Rating Scale (NRS) 0- 10. Possible score range from 0 (no pain) to 10 (worst pain ever ). The assessment of pain intensity, in patients on mechanical ventilation, will be done by: Behavioral Pain Scale, through facial expression (score 1-4), upper limb movement (score 1-5) and compliance with mechanical ventilation (score 1-3). Possible score range from 3 (no pain) to 12 (maximum pain).
Time Frame
24 hours after the cardiac surgery.
Secondary Outcome Measure Information:
Title
Opioid consumption.
Description
Opioid used for the pain control. This will be noted in the medical record.
Time Frame
During the first 24 hours.
Other Pre-specified Outcome Measures:
Title
Time from the end of surgery to extubation.
Description
This interval will be observed if the patient is not extubated at the end of the surgery. This will be noted in the medical record.
Time Frame
During the first 24 hours.
Title
Bleeding.
Description
Bleeding after the surgery. This will be noted in the medical record.
Time Frame
During the first 24 hours.
Title
Cardiac arrhythmias.
Description
Occurrence of cardiac arrhythmias. This will be noted in the medical record.
Time Frame
During the first 24 hours.
Title
Serum creatinine and urea.
Description
The serum level of creatinine and urea will be observed, in the usual daily measure. This will be noted in the medical record.
Time Frame
During the first 24 hours.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients at least 18 years old and who are undergoing cardiac procedures (coronary artery bypass, valve replacement or combined procedure), with cardiopulmonary by- pass. Exclusion Criteria: Congenital heart disease Infective endocarditis Acute myocardial infarction (<two weeks) Pregnancy Cancer Left ventricle ejection fraction < 40% Cardiogenic shock Emergent procedure Use of vasopressor and/or inotrope, in the preoperative Liver disfunction Renal replacement therapy Nephrectomy Previous renal transplantation Patients who are participating in another clinical research
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Luiz Antônio Machado César
Phone
551126617585
Email
cappesq.adm@hc.fm.usp.br
First Name & Middle Initial & Last Name or Official Title & Degree
Lígia Ferreira dos santos
Phone
558399189-6525
Email
ligiafs1@usp.br
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luiz Antônio Machado César
Organizational Affiliation
University of São Paulo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nova Esperança University Hospital
City
João Pessoa
State/Province
Paraíba
ZIP/Postal Code
58.015-345
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Luiz Antônio Machado César
Phone
551126617585
Email
cappesq.adm@hc.fm.usp.br
First Name & Middle Initial & Last Name & Degree
Lígia Ferreira dos santos
Phone
5583991896525
Email
ligiafs1@usp.br
First Name & Middle Initial & Last Name & Degree
Luiz Antônio Machado César
First Name & Middle Initial & Last Name & Degree
Lígia Ferreira dos Santos
Facility Name
Heart Institute (InCor), Univ. of Sao Paulo Medical School
City
Sao Paulo
ZIP/Postal Code
05403000
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Luiz A Machado Cesar, Phd, MD
Phone
551130695387
Email
luiz.cesar@incor.usp.br
First Name & Middle Initial & Last Name & Degree
Bruno M Mioto, MD
Phone
551130695437
Email
brunomioto@gmail.com
First Name & Middle Initial & Last Name & Degree
Bruno M Mioto, MD
First Name & Middle Initial & Last Name & Degree
Miguel A Moretti, MD, PhD
First Name & Middle Initial & Last Name & Degree
Daniela Taratsouchi, nutricionist
First Name & Middle Initial & Last Name & Degree
Reynaldo V Amato, MD, PhD
First Name & Middle Initial & Last Name & Degree
Vera Lucia Tuda, Nurse

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
This will be decided, after data collection stars.
Citations:
PubMed Identifier
31303717
Citation
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Results Reference
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29678158
Citation
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Results Reference
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10735784
Citation
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Results Reference
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PubMed Identifier
1854025
Citation
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
30235728
Citation
Kotfis K, Strzelbicka M, Zegan-Baranska M, Safranow K, Brykczynski M, Zukowski M, Ely EW; POL-BPS Study Group. Validation of the behavioral pain scale to assess pain intensity in adult, intubated postcardiac surgery patients: A cohort observational study - POL-BPS. Medicine (Baltimore). 2018 Sep;97(38):e12443. doi: 10.1097/MD.0000000000012443.
Results Reference
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PubMed Identifier
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Citation
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Results Reference
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Citation
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Efficacy and Safety of Dexmedetomidine in the Analgesic Prophylaxis , in Patients Undergoing Cardiovascular Surgery

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