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Effectiveness of Wound Drains for the Prevention Of Surgical sITe infectION (POSITION)

Primary Purpose

Surgical Site Infection, Gynecologic Cancer, Wound Drain

Status
Recruiting
Phase
Not Applicable
Locations
Greece
Study Type
Interventional
Intervention
Surgical drain
Sponsored by
National and Kapodistrian University of Athens
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Surgical Site Infection

Eligibility Criteria

30 Years - 85 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

This prospective randomized study will include obese (BMI> 35) patients who will undergo primary surgery for ovarian or endometrial cancer

Exclusion Criteria:

Immunodeficient patients (systemic disease including HIV infection, systemic lupus erythematosus etc) Patients with hematologic diseases

Sites / Locations

  • Alexandra HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Surgical drain

Control

Arm Description

In this arm participants a surgical drain (Redon type) will be inserted above the abdominal fascia prior to suture of the subcutaneous tissue and of the skin

In this arm the subcutaneous tissue and the skin of the surgical wound will be sutured without insertion of any type of drain

Outcomes

Primary Outcome Measures

Prevalence of surgical site infection
Surgical site infection will be defined as redness, swelling, pain, bleeding, or any discharge from the surgical site
Risk of surgical debridement of surgical site infection
Rates of surgical intervention to treat surgical site infection will be recorded

Secondary Outcome Measures

Risk of wound dehiscence
Rates of wound dehiscence (skin and/or fascia dehiscence) following surgical site infection or spontaneously (non-related to surgical site infection) will be recorded
Length and depth of wound dehiscence
In case of wound dehiscence the length and depth will be measured in cm
Risk of seroma formation
Rates of formation of seroma (defined as the collection of non-purulent fluid) in the surgical wound will be recorded.
Risk and duration of fever related to surgical site infection
Rates of fever related to surgical site infection and following exclusion of other causes will be reported in degrees of Celsius
Duration of antibiotic therapy directed against surgical site infection
The duration of post-operative use of antibiotics will be recorded in days
Duration of hospitalization
Duration of hospitalization will be recorded in days
Re-admission rates
Re-admission rates within 30 days will be reported
Interval to adjuvant therapy
The interval to adjuvant therapy (chemo- and/or radiotherapy) will be recorded in days

Full Information

First Posted
November 25, 2021
Last Updated
September 17, 2023
Sponsor
National and Kapodistrian University of Athens
Collaborators
Aristotle University Of Thessaloniki, Saint Savvas Anticancer Hospital, Metaxa Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05179122
Brief Title
Effectiveness of Wound Drains for the Prevention Of Surgical sITe infectION
Acronym
POSITION
Official Title
A Randomized Trial of Abdominal Wound Drainage in Obese Gynecologic Oncology Patients
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2021 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
January 15, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National and Kapodistrian University of Athens
Collaborators
Aristotle University Of Thessaloniki, Saint Savvas Anticancer Hospital, Metaxa Hospital

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
The aim of the present randomized trial is to assess the efficacy of wound drains in terms of reducing the rates of surgical site infection in obese patients with gynecological cancer.
Detailed Description
Many prophylactic methods have been suggested for the treatment of surgical wound infections, including the prolonged administration of antibiotics as well as the use of subcutaneous tissue drainage, the use of which has been shown to be particularly effective in overweight patients. While its importance seems to be moderate in obese patients as well as those that suffer from malignant disease, to date, it remains unknown if wound drains may help reduce the rates of surgical site infection in obese patients that suffer from cancer. In the field of gynecological oncology data are limited to anachronistic studies whose methodological value is limited; hence, guidelines are primarily based in data of high risk of bias as to date, the value of subcutaneous tissue drainage in obese women undergoing surgery for gynecological cancer has not been documented in a large randomized study. Considering the significant impact of surgical site infection on the interval to adjuvant therapy (as patients with infectious diseases cannot receive chemotherapy or radiotherapy), it becomes evident that every effort has to be made in order to help reduce the rates of SSI to help maintain acceptable intervals that will ensure appropriate care of patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Surgical Site Infection, Gynecologic Cancer, Wound Drain

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
The statistician involved in the statistical analyses of results will be blinded to the arm of treatment
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Surgical drain
Arm Type
Experimental
Arm Description
In this arm participants a surgical drain (Redon type) will be inserted above the abdominal fascia prior to suture of the subcutaneous tissue and of the skin
Arm Title
Control
Arm Type
No Intervention
Arm Description
In this arm the subcutaneous tissue and the skin of the surgical wound will be sutured without insertion of any type of drain
Intervention Type
Procedure
Intervention Name(s)
Surgical drain
Intervention Description
In this arm a surgical drain will be inserted prior to surgical wound closure
Primary Outcome Measure Information:
Title
Prevalence of surgical site infection
Description
Surgical site infection will be defined as redness, swelling, pain, bleeding, or any discharge from the surgical site
Time Frame
Within 30 days
Title
Risk of surgical debridement of surgical site infection
Description
Rates of surgical intervention to treat surgical site infection will be recorded
Time Frame
Within 30 days
Secondary Outcome Measure Information:
Title
Risk of wound dehiscence
Description
Rates of wound dehiscence (skin and/or fascia dehiscence) following surgical site infection or spontaneously (non-related to surgical site infection) will be recorded
Time Frame
Within 30 days
Title
Length and depth of wound dehiscence
Description
In case of wound dehiscence the length and depth will be measured in cm
Time Frame
Within 30 days
Title
Risk of seroma formation
Description
Rates of formation of seroma (defined as the collection of non-purulent fluid) in the surgical wound will be recorded.
Time Frame
Within 30 days
Title
Risk and duration of fever related to surgical site infection
Description
Rates of fever related to surgical site infection and following exclusion of other causes will be reported in degrees of Celsius
Time Frame
Within 30 days
Title
Duration of antibiotic therapy directed against surgical site infection
Description
The duration of post-operative use of antibiotics will be recorded in days
Time Frame
Within 30 days
Title
Duration of hospitalization
Description
Duration of hospitalization will be recorded in days
Time Frame
Within 30 days
Title
Re-admission rates
Description
Re-admission rates within 30 days will be reported
Time Frame
Within 30 days
Title
Interval to adjuvant therapy
Description
The interval to adjuvant therapy (chemo- and/or radiotherapy) will be recorded in days
Time Frame
Within 30 days
Other Pre-specified Outcome Measures:
Title
Overall survival
Description
3-year survival rate
Time Frame
3-year
Title
Overall survival
Description
5-year survival rate
Time Frame
5-year

10. Eligibility

Sex
Female
Gender Based
Yes
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: This prospective randomized study will include obese (BMI> 35) patients who will undergo primary surgery for ovarian or endometrial cancer Exclusion Criteria: Immunodeficient patients (systemic disease including HIV infection, systemic lupus erythematosus etc) Patients with hematologic diseases
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Vasilios Pergialiotis, MD
Phone
+306947326459
Email
pergialiotis@yahoo.com
First Name & Middle Initial & Last Name or Official Title & Degree
Dimitrios Haidopoulos, Assoc Prof
Email
dimitrioshaidopoulos@yahoo.com
Facility Information:
Facility Name
Alexandra Hospital
City
Athens
State/Province
Attika
ZIP/Postal Code
11528
Country
Greece
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dimitrios Haidopoulos, MD
Phone
+302132162291
Email
dimitrioshaidopoulos@gmail.com
First Name & Middle Initial & Last Name & Degree
George Vorgias, MD
First Name & Middle Initial & Last Name & Degree
Dimitrios Papatheodorou, MD
First Name & Middle Initial & Last Name & Degree
Dimitrios Tsolakids, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
24681712
Citation
Mahdi H, Gojayev A, Buechel M, Knight J, SanMarco J, Lockhart D, Michener C, Moslemi-Kebria M. Surgical site infection in women undergoing surgery for gynecologic cancer. Int J Gynecol Cancer. 2014 May;24(4):779-86. doi: 10.1097/IGC.0000000000000126.
Results Reference
background
PubMed Identifier
21324517
Citation
Nugent EK, Hoff JT, Gao F, Massad LS, Case A, Zighelboim I, Mutch DG, Thaker PH. Wound complications after gynecologic cancer surgery. Gynecol Oncol. 2011 May 1;121(2):347-52. doi: 10.1016/j.ygyno.2011.01.026. Epub 2011 Feb 15.
Results Reference
background
PubMed Identifier
26783556
Citation
Manzoor B, Heywood N, Sharma A. Review of Subcutaneous Wound Drainage in Reducing Surgical Site Infections after Laparotomy. Surg Res Pract. 2015;2015:715803. doi: 10.1155/2015/715803. Epub 2015 Dec 13.
Results Reference
background
PubMed Identifier
31923876
Citation
Pergialiotis V, Haidopoulos D, Tzortzis AS, Antonopoulos I, Thomakos N, Rodolakis A. The impact of waiting intervals on survival outcomes of patients with endometrial cancer: A systematic review of the literature. Eur J Obstet Gynecol Reprod Biol. 2020 Mar;246:1-6. doi: 10.1016/j.ejogrb.2020.01.004. Epub 2020 Jan 7.
Results Reference
background
PubMed Identifier
28209490
Citation
Steiner HL, Strand EA. Surgical-site infection in gynecologic surgery: pathophysiology and prevention. Am J Obstet Gynecol. 2017 Aug;217(2):121-128. doi: 10.1016/j.ajog.2017.02.014. Epub 2017 Feb 14.
Results Reference
result

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Effectiveness of Wound Drains for the Prevention Of Surgical sITe infectION

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