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Povidone-iodine and the Normal Saline Cleaning the Incision for the SSIs

Primary Purpose

Surgical Site Infections, Gastric Cancer, Dehiscence of Laparotomy Wound

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Group A (povidone-iodine wash the surgical incision)
Group B (normal saline wash the surgical incision)
Sponsored by
West China Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Surgical Site Infections focused on measuring gastric cancer, gastrectomy, laparotomy, SSIs, povidone-iodine, normal saline

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Preoperative endoscopy and biopsy confirmed gastric adenocarcinoma, and predictively feasible of conventional open total gastrectomy or subtotal gastrectomy;
  2. Predictively resectable diseases, of preoperative staging JGCA 14th Edition cT1N0M0-T4aN+M0, Ia-IIIc stage
  3. Age:≤75 years, or ≥18 years;
  4. Without serious disease and malignance disease;
  5. WHO performance score ≤2, ASA score ≤3;
  6. No limit to sexual and race;
  7. Informed consent required.

Exclusion Criteria:

  1. Emergence operation, because of obstruction, perforate, acute hemorrhage and et al;
  2. Patients with laparoscopic or laparoscopic-assisted gastrectomy
  3. Patients with other severe complications cannot tolerate surgery: such as severe heart and lung diseases, heart function below clinical stage 2, uncontrollable hypertension, pulmonary infection, moderate to severe COPD, chronic bronchitis, severe diabetes and / or renal insufficiency, severe hepatitis and / or function below the rank of CHILD B grade, and severe malnutrition, etc;
  4. Patients treated with neoadjuvant chemotherapy or radiation therapy which might affect the efficacy observation;
  5. Severity mental diseases;
  6. Primary lesion cannot be resected in the pattern of transabdominal gastrectomy, but for Whipple's procedure, or with a transthoracic approach surgery;
  7. After signature the Clinical trial agreement, patients and their agent will quit the trial.

Sites / Locations

  • West China HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Group A (povidone-iodine group)

Group B (normal saline group)

Arm Description

The surgical incision is washed by the mixed solution with 400ml 9% normal saline and 100ml 5% povidone-iodine solution. We declare that we have no conflicts of interest.

The surgical incision is washed by the 500ml 0.9% normal saline. We declare that we have no conflicts of interest.

Outcomes

Primary Outcome Measures

Superficial incisional surgical site infections
The ceriteria for defining a surgical site infection adopt the defination of the Guideline for Prevention of Surgical Site Infection, 1999. Centers for Disease Control and Prevention (CDC) Hospital Infection Control Practices Advisory Committee.Am J Infect Control. 1999;27(2):97-132; quiz 133-4; discussion 96.

Secondary Outcome Measures

Full Information

First Posted
December 7, 2014
Last Updated
December 7, 2017
Sponsor
West China Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02436395
Brief Title
Povidone-iodine and the Normal Saline Cleaning the Incision for the SSIs
Official Title
Comparison the Influence of the Povidone-iodine or the Normal Saline Cleaning the Incision for the Incidence of the Surgical Site Infections for Gastric Cancer Patients With Gastrectomy- Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2017
Overall Recruitment Status
Unknown status
Study Start Date
May 2015 (Actual)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
December 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
West China Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Surgical site infections (SSIs) is one of the most common complications of upper abdominal surgery. Previous studies found that type of surgical incision, emergency operation or not, surgical duration, age of patient, body mass index, malignance duration, malnutrition, complications (diabetes, shock, anemia et al) and drug (Long-term use of corticosteroids) are closely associated with the incidence of SSIs. The general incidence rate of SSIs was about 5% to 40%, although using the preoperative skin disinfectant and other methods to prevent and reduce the SSIs. And for the gastrointestinal surgery, due to the potential risk of infection, SSIs is an important problem which cannot be ignored. On the other hand, gastric cancer is one of the most common digestive system tumors, and gastrectomy is the primary therapeutic options. Therefore, it is important to compare the whether the different liquid (1% povidone-iodine solution or the 0.9% normal saline) wash the incision can influent the incidence of the SSIs.
Detailed Description
Standard Operating Procedure (SOP) Preoperative evaluation Patients satisfied with inclusion/exclusion criteria will be informed to join in the clinical study and signature the inform consent. Randomization: Preoperative evaluation found that total or subtotal gastrectomy can be performed, the case will entrance into the Randomization period. Random numbers are computer-generated, with the third party applications. Procedures: The surgical treatments is adopted the conventional open total or subtotal gastrectomy according to the Japanese Gastric Cancer treatments guidelines, 2010, Version 3. Patients in the Group A using the mixed solution with 400ml,0.9% normal saline and 100 ml,5%, povidone-iodine solution, and patients in the Group B with 500ml 0.9% normal saline solution to wash the abdominal surgical incision. Postoperative recovery: Postoperative recovery period need to collect those relevant parameters of all the patients. All the relevant parameters had definitely definition in the Case Report Form of this study which included the preoperative, intraoperative and postoperative clinicopathologic characteristics. Follow-up: Follow-up will last to the 30-day of the postoperative period. The postoperative complications is graded by the Clavien-Dindo classification. And the surgical site infections are the focus of this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Surgical Site Infections, Gastric Cancer, Dehiscence of Laparotomy Wound
Keywords
gastric cancer, gastrectomy, laparotomy, SSIs, povidone-iodine, normal saline

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
340 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group A (povidone-iodine group)
Arm Type
Experimental
Arm Description
The surgical incision is washed by the mixed solution with 400ml 9% normal saline and 100ml 5% povidone-iodine solution. We declare that we have no conflicts of interest.
Arm Title
Group B (normal saline group)
Arm Type
Experimental
Arm Description
The surgical incision is washed by the 500ml 0.9% normal saline. We declare that we have no conflicts of interest.
Intervention Type
Procedure
Intervention Name(s)
Group A (povidone-iodine wash the surgical incision)
Intervention Description
Gastric cancer patients underwent conventional open D2 total or subtotal gastrectomy and with povidone-iodine wash the surgical incision
Intervention Type
Procedure
Intervention Name(s)
Group B (normal saline wash the surgical incision)
Intervention Description
Gastric cancer patients underwent conventional open D2 total or subtotal gastrectomy and with normal saline wash the surgical incision
Primary Outcome Measure Information:
Title
Superficial incisional surgical site infections
Description
The ceriteria for defining a surgical site infection adopt the defination of the Guideline for Prevention of Surgical Site Infection, 1999. Centers for Disease Control and Prevention (CDC) Hospital Infection Control Practices Advisory Committee.Am J Infect Control. 1999;27(2):97-132; quiz 133-4; discussion 96.
Time Frame
30-day of postoperative duration

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Preoperative endoscopy and biopsy confirmed gastric adenocarcinoma, and predictively feasible of conventional open total gastrectomy or subtotal gastrectomy; Predictively resectable diseases, of preoperative staging JGCA 14th Edition cT1N0M0-T4aN+M0, Ia-IIIc stage Age:≤75 years, or ≥18 years; Without serious disease and malignance disease; WHO performance score ≤2, ASA score ≤3; No limit to sexual and race; Informed consent required. Exclusion Criteria: Emergence operation, because of obstruction, perforate, acute hemorrhage and et al; Patients with laparoscopic or laparoscopic-assisted gastrectomy Patients with other severe complications cannot tolerate surgery: such as severe heart and lung diseases, heart function below clinical stage 2, uncontrollable hypertension, pulmonary infection, moderate to severe COPD, chronic bronchitis, severe diabetes and / or renal insufficiency, severe hepatitis and / or function below the rank of CHILD B grade, and severe malnutrition, etc; Patients treated with neoadjuvant chemotherapy or radiation therapy which might affect the efficacy observation; Severity mental diseases; Primary lesion cannot be resected in the pattern of transabdominal gastrectomy, but for Whipple's procedure, or with a transthoracic approach surgery; After signature the Clinical trial agreement, patients and their agent will quit the trial.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wei-Han Zhang, M.D.
Email
weihanwch@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jian-Kun Hu, M.D. Ph.D.
Organizational Affiliation
West China Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
West China Hospital
City
Chengdu
State/Province
Sichuan
ZIP/Postal Code
610041
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wei-Han Zhang, M.D.
Email
weihanwch@126.com
First Name & Middle Initial & Last Name & Degree
Xin-Zu Chen, M.D.
Email
chen_xz_wch_scu@126.com
First Name & Middle Initial & Last Name & Degree
Jian-Kun Hu, M.D.Ph.D.
First Name & Middle Initial & Last Name & Degree
Wei-Han Zhang, M.D.
First Name & Middle Initial & Last Name & Degree
Xin-Zu Chen, M.D.

12. IPD Sharing Statement

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Povidone-iodine and the Normal Saline Cleaning the Incision for the SSIs

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