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Combined Air-plasma Flow and Nitric Oxide Therapy in Cardiac Surgery

Primary Purpose

Mediastinitis

Status
Active
Phase
Not Applicable
Locations
Russian Federation
Study Type
Interventional
Intervention
NO-based treatment of sterno-mediastinitis
Treatment of sterno-mediastinitis
Sponsored by
Tomsk National Research Medical Center of the Russian Academy of Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mediastinitis focused on measuring plasma, endogenous nitric oxide, infectious complications, mediastinitis

Eligibility Criteria

40 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients who underwent heart and great vessels surgery with confirmed laboratory, bacteriological, instrumental tests, as well as the presence of clinical signs of sterno-mediastinitis.
  • Signed informed consent to participate in the study

Exclusion Criteria:

  • Patients who underwent heart and great vessels surgery not through a median sternotomy.
  • Patients who have signs of inconsistency of sutures or any other wound complications, but there are no clinical, laboratory, bacteriological data indicating infection of the postoperative wound.
  • No informed consent to participate in the study.

Sites / Locations

  • TomskNRMC

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Plasma

Standard therapy

Arm Description

(the treatment of sterno-mediastinitis was carried out using a combined method of air-plasma flow and NO therapy)

(patients who were treated for sterno-mediastinitis according to clinical guidelines, the main method of which is a permanent irrigation and aspiration flow drainage method, as well as a Vacuum Assisted Closure (VAC) system of dressings for vacuum drainage)

Outcomes

Primary Outcome Measures

Death
In-hospital mortality rate (%)
Re-infection of the wound
Rate wound re-infection (%)
Skin suture incompetence
Rate of skin suture incompetence (%) due to lack of tissue repair
Recovery
Rate of full recovery (%)

Secondary Outcome Measures

Full Information

First Posted
October 30, 2020
Last Updated
January 24, 2023
Sponsor
Tomsk National Research Medical Center of the Russian Academy of Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT04617353
Brief Title
Combined Air-plasma Flow and Nitric Oxide Therapy in Cardiac Surgery
Official Title
Experience With the Combined Method of Air-plasma Flow and Nitric Oxide Therapy in the Prevention and Treatment of Wound Infectious Complications in Cardiac Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
March 14, 2017 (Actual)
Primary Completion Date
December 20, 2021 (Actual)
Study Completion Date
December 20, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tomsk National Research Medical Center of the Russian Academy of Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In cardiovascular surgery, the most common and serious complication is postoperative wound infection. The most formidable wound complication is mediastinitis, the frequency of which varies from 1 to 3%. Currently, mortality in this group of patients varies from 3.5 to 58.3%. In this regard, the relevance of developing new methods for the prevention and treatment of infectious wound complications is beyond doubt. In this study, it is supposed to examine and evaluate the effectiveness of the combined effects of air-plasma flow and nitric oxide in the treatment of postoperative infectious complications in cardiac surgery.
Detailed Description
One of the most common and serious complications in cardiovascular surgery is sternal wound infection. According to many authors, the incidence of infectious complications after sternotomy ranges from 0.4% to 15% . Superficial infection of the anterior chest wall after median sternotomy occurs in 0.4-15% . Typically, this complication is detected within the first two weeks (on average, about seven days). The most formidable wound infectious complication is mediastinitis. According to various authors, the incidence of mediastinitis varies from 1 to 3%. Mortality in this group of patients reaches 39% . Until now, the only effective and generally accepted method for treating patients with mediastinitis has been antibiotic therapy in combination with surgical intervention. The options for antibiotic therapy remain generally accepted and their effectiveness is not discussed, however, there are many options for various types of surgical treatment. Their main principle is to perform resternotomy, necrosectomy, followed by reosteosynthesis of the sternum and the installation of permanent irrigation and aspiration, flow-through drainage. Despite this, the mortality rate in this pathology remains invariably high. In this regard, issues related to the development of new medical technologies, methods for prevention and treatment of infectious wound complications do not lose their relevance at the present time. During the study, it is supposed to use an original method developed for the prevention, as well as for the treatment of wound infectious complications. The advantage of the investigator's proposed original method of treating mediastinitis is in the combined effect of thermal (air-plasma flow) and biochemical (effect of NO on wound surfaces) by stimulating the processes of regeneration and repair. Also, for obvious reasons, resistance cannot arise to it, which is relevant in the context of the widespread transmission of nosocomial infections, especially in large hospitals, such as modern cardiology dispensaries. As a result of the work, the cases of infectious wound complications in the early postoperative period, the total number of bed-days spent, the time spent in the ICU, the duration of mechanical ventilation, laboratory parameters: red blood cell count, coagulation system, markers of infection and inflammation, state of sepsis, determination of how fast the bone tissue reparation is, CT scan of the chest, sternum, examination of the bacterial flora and bacterial contamination of the postoperative wound will be assessed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mediastinitis
Keywords
plasma, endogenous nitric oxide, infectious complications, mediastinitis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patient enrollment according to the inclusion criteria. Carrying out medical manipulations according to the group inclusion criteria. Efficiency control based on the clinical course of the disease, instrumental and laboratory study methods. After the patient is discharged from the hospital, a follow-up examination after 12 months, including an objective examination, a spiral computed tomography of the chest organs. Complete blood count, general urine test, biochemistry blood test. Comparison of the main clinical and laboratory parameters between patients of both groups: the total number of bed-days spent, the time spent in the ICU, the duration of mechanical ventilation, laboratory parameters: red blood cell count, coagulation system, markers of infection and inflammation, state of sepsis, determination of how fast the bone tissue reparation is. CT scan of the chest, sternum, examination of the bacterial flora and bacterial contamination of the postoperative wound
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Plasma
Arm Type
Experimental
Arm Description
(the treatment of sterno-mediastinitis was carried out using a combined method of air-plasma flow and NO therapy)
Arm Title
Standard therapy
Arm Type
Other
Arm Description
(patients who were treated for sterno-mediastinitis according to clinical guidelines, the main method of which is a permanent irrigation and aspiration flow drainage method, as well as a Vacuum Assisted Closure (VAC) system of dressings for vacuum drainage)
Intervention Type
Procedure
Intervention Name(s)
NO-based treatment of sterno-mediastinitis
Intervention Description
Preparation of a postoperative wound in case of infectious complications. A mandatory sampling material for culture and antibiotic sensitivity is collected before and after the air plasma flow treatment. Direct effect of the air-plasma flow on the entire wound surface in sterilization mode with an exposure of 2-3 minutes for each surgical wound, until the level of bacterial contamination decreases to 10-5 and below. The technique of using air-plasma flow when closing a wound after preventing infectious complications in it. In the postoperative period, daily air-plasma flow treatment in sterilization mode along the suture line for 3 minutes. Penetrating drainage NO supply in the biological stimulation mode daily for 10 days, with an exposure of 1-2 minutes up to 10 days, with a volume of up to 2 liters per minute. Collecting wound culture from the drainage containers on 1-3-7-12 days to detect pathogens and the bacterial number.
Intervention Type
Procedure
Intervention Name(s)
Treatment of sterno-mediastinitis
Intervention Description
patients who were treated for sterno-mediastinitis according to clinical guidelines, the main method of which is a permanent irrigation and aspiration flow drainage method, as well as a Vacuum Assisted Closure (VAC) system of dressings for vacuum drainage
Primary Outcome Measure Information:
Title
Death
Description
In-hospital mortality rate (%)
Time Frame
30 days
Title
Re-infection of the wound
Description
Rate wound re-infection (%)
Time Frame
30 days
Title
Skin suture incompetence
Description
Rate of skin suture incompetence (%) due to lack of tissue repair
Time Frame
30 days
Title
Recovery
Description
Rate of full recovery (%)
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients who underwent heart and great vessels surgery with confirmed laboratory, bacteriological, instrumental tests, as well as the presence of clinical signs of sterno-mediastinitis. Signed informed consent to participate in the study Exclusion Criteria: Patients who underwent heart and great vessels surgery not through a median sternotomy. Patients who have signs of inconsistency of sutures or any other wound complications, but there are no clinical, laboratory, bacteriological data indicating infection of the postoperative wound. No informed consent to participate in the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mikhail Kuznetsov, PhD
Organizational Affiliation
Tomsk National Research Medical Center of the Russian Academy of Sciences
Official's Role
Study Chair
Facility Information:
Facility Name
TomskNRMC
City
Tomsk
State/Province
Tomskay Oblast
ZIP/Postal Code
634012
Country
Russian Federation

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Deidentified individual participant data (text, tables, figures, and appendices), underlying the results of the trial, will be shared with researchers to achieve the aims in the approved proposal.
IPD Sharing Time Frame
Proposals may be submitted up to 36 months following publication of the results of the trial. After 36 months, the data will be available in the Center's data ware house but without investigator support other than deposited metadata.
IPD Sharing Access Criteria
Information regarding submitting proposals and accessing data may be requested from the principal investigator by e-mail.

Learn more about this trial

Combined Air-plasma Flow and Nitric Oxide Therapy in Cardiac Surgery

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