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External Negative Pressure Dressing System vs. Traditional Wound Dressing for Cesarean Section Incision in Obese Women.

Primary Purpose

Wound Dehiscence

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
External negative pressure dressing system (Yuwell 7E-A portable suction unit)
Sponsored by
Ain Shams Maternity Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Wound Dehiscence focused on measuring wound dehiscence, obesity, negative pressure therapy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Age: 18 or older
  • BMI: 30 or greater
  • undergoing Cesarean section through a Pfannenstiel incision

Exclusion Criteria:

  • Prolonged Rupture of membranes >18 hours
  • Intra amniotic infection
  • Severe anemia
  • Vasculopathies as in hypertension/pre-eclampsia, pregestational / gestational diabetes mellitus, smoking and substance abuse
  • Prolonged steroids therapy as in SLE, ITP
  • Intraoperative complications as bladder or bowel injury , placenta previa / accreta, difficult fetal extraction , ovarian cysts, pelvic abscess
  • Intra-abdominal or subcutaneous drain

Sites / Locations

  • AinShams maternity hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

standard dressing group

External negative pressure dressing system group

Arm Description

patients will receive sterile wound dressing of gauze and tape for 4 days.

patients will receive placement of a sterile dressing of gauze and occlusive adhesive over the closed incision. The dressing's tubing will then be attached to a compact, portable negative-pressure therapy unit (Yuwell 7E-A portable suction unit) that will deliver -80 mm Hg of continuous pressure to the dressing and will remove exudates into a disposable canister for 4 days.

Outcomes

Primary Outcome Measures

incidence of wound dehiscence
separation of the incision line prior to complete healing resulting in an open wound.

Secondary Outcome Measures

post operative pain
post-operative pain assessed by Wong-Baker Faces pain rating scale,from 0=no pain to 10=maximal pain
length of hospital stay
days spent admitted to the hospital
the need for re-admission
if the patient encountered surgical site infection requiring re admission to the hospital
further need for additional antibiotics
if the surgical site infection required additional post operative antibiotics
peri-incision blistering
if any skin blistering occurs under the occlusive adhesive layer
patient mobility
if attachment to a negative pressure pump affects patients mobility
surgical site infection
as defined by the CDC

Full Information

First Posted
June 14, 2020
Last Updated
February 17, 2021
Sponsor
Ain Shams Maternity Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04434820
Brief Title
External Negative Pressure Dressing System vs. Traditional Wound Dressing for Cesarean Section Incision in Obese Women.
Official Title
External Negative Pressure Dressing System (ENPDS) vs. Traditional Wound Dressing for Cesarean Section Incision in Obese Women.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
August 3, 2020 (Actual)
Primary Completion Date
February 3, 2021 (Actual)
Study Completion Date
February 4, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ain Shams Maternity Hospital

4. Oversight

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

5. Study Description

Brief Summary
Obesity is associated with increased cesarean section delivery rates and surgical site infections with associated increased post-operative morbidity, post-operative pain and length of hospital stay. Negative pressure wound therapy (NPWT) technology could be used as a prophylactic measure to reduce surgical site infections in obese women undergoing cesarean section by immediate postoperative application in clean-contaminated, closed surgical incisions.
Detailed Description
Obesity, defined as body mass index (BMI, calculated as weight (kg)/ [height (m)] 2) of 30 or greater, is a common medical comorbidity of pregnancy affecting one third of reproductive-aged women. Maternal obesity is also a well-recognized risk factor for dysfunctional labor and cesarean delivery with a cesarean section rate of 33% in obese women with BMI of 30 or greater and 43% in women with BMIs of 40 or greater. Obesity is an independent risk factor for post-operative surgical site infection. The risk of post-cesarean surgical site infection has been shown to double for every 5 unit increase in body mass index (BMI) above 30 kg/m , occurring in about 10% of obese women undergoing caesarean section despite prophylactic strategies (e.g. antibiotics). This can be explained partly by a decreased blood flow in adipose tissue and an obesity-associated inflammation causing vascular dysfunction, which results in a local hypoxic response. Hypoxia impairs oxidative bacterial killing and leads to an increased risk of surgical site infection. Wound healing is a sequence of physiologic events that include inflammation, epithelialization, fibroplasia, and maturation. Failure of wound healing at the surgical site can lead to seroma, hematoma, wound dehiscence, incisional hernia and surgical site infection. Surgical site infection SSI according to The Centers for Disease Control and Prevention is as an infection occurring within 30 days from the operative procedure in the part of the body where the surgery took place, where there is purulent drainage from incision, isolated organisms from the incision, dehiscence or deliberate opening by the surgeon when the patient has at least one sign or symptom of clinical infection: localized pain, edema, erythema, warmth and fever greater than 38 c (unless culture of incision is negative) or there is an abscess or other evidence of infection is found during examination of incision, reoperation, or pathologic or radiologic exam. SSIs is divided into incisional SSI and organ/space SSI. Incisional SSI is further divided into superficial and deep incisional SSI. Superficial Incisional Surgical Site Infection involves skin or subcutaneous tissue cellulitis, seroma, hematoma, wound healing disruption, or dehiscence. Deep Incisional Surgical Site Infection involves deep soft tissues such as fascia or muscle within incision. Organ/Space Surgical Site Infection involves any part of the anatomy other than the incision. SSI is associated with a maternal mortality rate of up to 3%. Wound complication, even if not accompanied by an infection, is a significant cause of postoperative morbidity following cesarean delivery. In addition to the increased cost of care, there is the inconvenience of therapy, increased postoperative pain and convalescence, as well as difficulty with activities of daily living. It is logical to employ novel risk reducing approaches including negative pressure wound therapy at the time of surgery that may prevent wound complications and to ensure that there is a demonstrable benefit to their use for wound complication prophylaxis. Negative pressure wound therapy (NPWT), also known as a vacuum assisted closure (VAC), involves the controlled application of sub-atmospheric pressure to the local wound environment, using a sealed wound dressing connected to a vacuum to promote healing by primary intention by reducing the risk of hematoma / seroma due to improved lymphatic drainage and reduces the risk of wound dehiscence by decreasing the lateral and shear stress on sutures and decreasing bacterial load and wound fluids and by increasing blood flow, oxygenation, angiogenesis, and epithelialization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Wound Dehiscence
Keywords
wound dehiscence, obesity, negative pressure therapy

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Basic information included age, ethnicity, weight, height, body mass index (BMI). Full obstetric, medical and surgical history. Informed written consent will be obtained Patients will receive standard preoperative antibiotic prophylaxis Wound dressing will be applied in a sterile fashion after primary closure of the Pfannenstiel incision closure by interrupted PROLENE Polypropylene Sutures The intervention group: placement of a sterile multilayer dressing (wicking fabric, reticulated foam, and occlusive adhesive). The dressing's tubing will then be attached to a (Yuwell 7E-A portable suction unit) that will deliver 125 mm Hg of continuous pressure to the dressing for 4 days. The comparison group: traditional sterile wound dressing of gauze and tape for 4 days. Post-operative data including: type of dressing used, postoperative hemoglobin, degree of pain, length of hospital stay, readmission for surgical site infection and the type of the surgical site infection.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
260 (Actual)

8. Arms, Groups, and Interventions

Arm Title
standard dressing group
Arm Type
No Intervention
Arm Description
patients will receive sterile wound dressing of gauze and tape for 4 days.
Arm Title
External negative pressure dressing system group
Arm Type
Active Comparator
Arm Description
patients will receive placement of a sterile dressing of gauze and occlusive adhesive over the closed incision. The dressing's tubing will then be attached to a compact, portable negative-pressure therapy unit (Yuwell 7E-A portable suction unit) that will deliver -80 mm Hg of continuous pressure to the dressing and will remove exudates into a disposable canister for 4 days.
Intervention Type
Device
Intervention Name(s)
External negative pressure dressing system (Yuwell 7E-A portable suction unit)
Intervention Description
A portable suction unit that will deliver 125 mm Hg of continuous pressure to the dressing and will remove exudates into a disposable canister for 4 days.
Primary Outcome Measure Information:
Title
incidence of wound dehiscence
Description
separation of the incision line prior to complete healing resulting in an open wound.
Time Frame
till 30 days post operative
Secondary Outcome Measure Information:
Title
post operative pain
Description
post-operative pain assessed by Wong-Baker Faces pain rating scale,from 0=no pain to 10=maximal pain
Time Frame
till 30 days post operative
Title
length of hospital stay
Description
days spent admitted to the hospital
Time Frame
till 30 days post operative
Title
the need for re-admission
Description
if the patient encountered surgical site infection requiring re admission to the hospital
Time Frame
till 30 days post operative
Title
further need for additional antibiotics
Description
if the surgical site infection required additional post operative antibiotics
Time Frame
till 30 days post operative
Title
peri-incision blistering
Description
if any skin blistering occurs under the occlusive adhesive layer
Time Frame
till 30 days post operative
Title
patient mobility
Description
if attachment to a negative pressure pump affects patients mobility
Time Frame
4 days
Title
surgical site infection
Description
as defined by the CDC
Time Frame
30 days post operative

10. Eligibility

Sex
Female
Gender Based
Yes
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age: 18 or older BMI: 30 or greater undergoing Cesarean section through a Pfannenstiel incision Exclusion Criteria: Prolonged Rupture of membranes >18 hours Intra amniotic infection Severe anemia Vasculopathies as in hypertension/pre-eclampsia, pregestational / gestational diabetes mellitus, smoking and substance abuse Prolonged steroids therapy as in SLE, ITP Intraoperative complications as bladder or bowel injury , placenta previa / accreta, difficult fetal extraction , ovarian cysts, pelvic abscess Intra-abdominal or subcutaneous drain
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dalia M Mokhtar, MBBCh
Organizational Affiliation
resident of obstetrics and gynecology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Marwan O Elkady, MD
Organizational Affiliation
Lecturer of obstetrics and gynecology
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Mohammed S El Sokkary, MD
Organizational Affiliation
Professor of obstetrics and gynecology
Official's Role
Study Chair
Facility Information:
Facility Name
AinShams maternity hospital
City
Cairo
State/Province
Al-Waili
ZIP/Postal Code
11658
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
patient's age ,ethnicity,gravidity,parity,gestational age ,previous cesarean section, previous surgeries,weight, height,BMI,pre/post operative haemoglobin,degree of post operative pain,incidence and type of surgical site infection,length of hospital stay, need for re-admission,need for additional antibiotics
IPD Sharing Time Frame
after completing the study and henceforth .
IPD Sharing Access Criteria
everyone can review the IPD on this site for any type of analysis they desire .
Citations:
PubMed Identifier
30066454
Citation
Hyldig N, Vinter CA, Kruse M, Mogensen O, Bille C, Sorensen JA, Lamont RF, Wu C, Heidemann LN, Ibsen MH, Laursen JB, Ovesen PG, Rorbye C, Tanvig M, Joergensen JS. Prophylactic incisional negative pressure wound therapy reduces the risk of surgical site infection after caesarean section in obese women: a pragmatic randomised clinical trial. BJOG. 2019 Apr;126(5):628-635. doi: 10.1111/1471-0528.15413. Epub 2018 Sep 7.
Results Reference
background
PubMed Identifier
24056202
Citation
Mark KS, Alger L, Terplan M. Incisional negative pressure therapy to prevent wound complications following cesarean section in morbidly obese women: a pilot study. Surg Innov. 2014 Aug;21(4):345-9. doi: 10.1177/1553350613503736. Epub 2013 Sep 20.
Results Reference
background
PubMed Identifier
28824992
Citation
Orth TA, Gerkovich MM, Heitmann E, Overcash J, Gibbs C, Parrish M. Cesarean Delivery with External Negative Pressure Dressing System: A Retrospective Cohort Study. Surg J (N Y). 2016 Jul 20;2(3):e59-e65. doi: 10.1055/s-0036-1585470. eCollection 2016 Jul.
Results Reference
background
PubMed Identifier
25234139
Citation
Scalise A, Tartaglione C, Bolletta E, Calamita R, Nicoletti G, Pierangeli M, Grassetti L, Di Benedetto G. The enhanced healing of a high-risk, clean, sutured surgical incision by prophylactic negative pressure wound therapy as delivered by Prevena Customizable: cosmetic and therapeutic results. Int Wound J. 2015 Apr;12(2):218-23. doi: 10.1111/iwj.12370. Epub 2014 Sep 19.
Results Reference
background
PubMed Identifier
29016508
Citation
Smid MC, Dotters-Katz SK, Grace M, Wright ST, Villers MS, Hardy-Fairbanks A, Stamilio DM. Prophylactic Negative Pressure Wound Therapy for Obese Women After Cesarean Delivery: A Systematic Review and Meta-analysis. Obstet Gynecol. 2017 Nov;130(5):969-978. doi: 10.1097/AOG.0000000000002259.
Results Reference
background
PubMed Identifier
28749874
Citation
Todd B. New CDC Guideline for the Prevention of Surgical Site Infection. Am J Nurs. 2017 Aug;117(8):17. doi: 10.1097/01.NAJ.0000521963.77728.c0.
Results Reference
background
PubMed Identifier
31396673
Citation
Wells CI, Ratnayake CBB, Perrin J, Pandanaboyana S. Prophylactic Negative Pressure Wound Therapy in Closed Abdominal Incisions: A Meta-analysis of Randomised Controlled Trials. World J Surg. 2019 Nov;43(11):2779-2788. doi: 10.1007/s00268-019-05116-6.
Results Reference
background
PubMed Identifier
28255256
Citation
Zuarez-Easton S, Zafran N, Garmi G, Salim R. Postcesarean wound infection: prevalence, impact, prevention, and management challenges. Int J Womens Health. 2017 Feb 17;9:81-88. doi: 10.2147/IJWH.S98876. eCollection 2017.
Results Reference
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External Negative Pressure Dressing System vs. Traditional Wound Dressing for Cesarean Section Incision in Obese Women.

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