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Prospective Study on Cesarean Wound Outcomes

Primary Purpose

Surgical Site Infection, Cosmetic Appearance of Cesarean Scar, Post Operative Pain

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Silver-impregnated dressing
Telfa pad dressing
Sponsored by
University of South Florida
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Surgical Site Infection focused on measuring cesarean section incisions, silver, c-section, wound infection, scar appearance, post operative pain

Eligibility Criteria

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

Inclusion Criteria:

  • Age 18 or older
  • Elective and emergent cesarean deliveries
  • Primary and repeat cesarean sections
  • Transverse skin incisions (Pfannenstiel)
  • Low transverse uterine incisions
  • Patients with or without the diagnosis of chorioamnionitis with antibiotic treatment prior to or after the delivery of the baby
  • Single and multiple gestations
  • Able and willing to provide written informed consent

Exclusion Criteria:

  • Patients that did not receive routine prophylactic dose of antibiotics in the operating room.
  • Skin incisions other than Pfannenstiel
  • Uterine incisions other than low transverse
  • Patients with known or discovered allergy to silver or nylon

Sites / Locations

  • USF Health South Tampa Center for Advanced Healthcare
  • Women's Center Operating Rooms at the Tampa General Hospital
  • USF Health Morsani Center for Advanced Healthcare

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Telfa pad dressing

Silver-impregnated dressing

Arm Description

Telfa pad dressing placed over Cesarean wound after skin closure; the dressing will be changed to a new Telfa pad dressing on post-operative day 2 which will remain on the incision through post-operative day 7.

Silver-impregnated dressing placed over Cesarean wound after skin closure; the dressing will be changed to saline-treated dressing on post-operative day 2 which will remain on the incision through post-operative day 7.

Outcomes

Primary Outcome Measures

Percentage of Patients Who Develop a Surgical Site Infection
A surgical site infection involving the skin and subcutaneous tissue is defined as either The presence of a purulent discharge from the wound on inspection, or Purulent discharge obtained from the wound after exploration based on the suspicion of the provider (erythema, swelling, heat or pain), or The presence of a seroma or hematoma discharge from the wound on inspection or after exploration that also involves isolation of an organism from an aseptically obtained culture based on suspicion of the provider (erythema, swelling, heat or pain). Seromas or hematomas with negative cultures will not be considered a surgical site infection.

Secondary Outcome Measures

Cosmetic Outcome of the Cesarean Section Incision
The following instruments will be used to determine the cosmetic outcome: • The Modified Vancouver scar scale Range of scale values are from 0-12 (0 indicating a better outcome)
Cosmetic Outcome of the Cesarean Section Incision
The following instruments will be used to determine the cosmetic outcome • The Modified Observer Scar Assessment Scale Range of scale values is from 5 - 50 ( the lower the score the better the outcome)

Full Information

First Posted
September 19, 2012
Last Updated
October 25, 2019
Sponsor
University of South Florida
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1. Study Identification

Unique Protocol Identification Number
NCT01697748
Brief Title
Prospective Study on Cesarean Wound Outcomes
Official Title
A Prospective Randomized Study Assessing Post Operative Wound Infections Along With Cosmetic Outcomes Using Silver Impregnated Dressings Compared to Conventional Dressings on Cesarean Section Incisions
Study Type
Interventional

2. Study Status

Record Verification Date
December 2012
Overall Recruitment Status
Completed
Study Start Date
September 2013 (undefined)
Primary Completion Date
August 2016 (Actual)
Study Completion Date
May 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of South Florida

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will investigate whether the placement of silver impregnated dressings beginning in the OR will improve wound healing in patients undergoing cesarean delivery compared to traditional Telfa pads. This study will also explore the presumed improvement in scar integrity when silver impregnated dressings are used compared to the Telfa pads. The study will compare the percentage of patients who develop a surgical site infection after application of silver impregnated dressings versus standard Telfa dressings. Investigators will also assess the cosmetic appearance and pain of the cesarean section scar at the patient's one week and 6 week post-operative visits.
Detailed Description
This is a randomized, prospective study involving 660 patients undergoing cesarean sections at Tampa General Hospital. The control group (n=330) will receive standard Telfa pad dressing and the treatment group (n=330) will receive the silver impregnated dressing. The primary objective is to compare the percentage of patients who develop a surgical site infection between the two groups at the 1-week and 6-weeks post operative visits. The secondary objective is to assess the cosmetic outcome of the cesarean incision observed at the 1-week and 6-week post-operative visits. A plastic surgery investigator will also conduct a blinded assessment of cosmetic outcome by review of photographs taken of the wounds at 1-week and 6-weeks.The tertiary objective is to evaluate the amount of narcotic and non narcotic medicine consumed during the hospitalization and query the patient with regards to pain involving the cesarean wound at 1 and 6 week post-operative visits

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Surgical Site Infection, Cosmetic Appearance of Cesarean Scar, Post Operative Pain
Keywords
cesarean section incisions, silver, c-section, wound infection, scar appearance, post operative pain

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
660 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Telfa pad dressing
Arm Type
Placebo Comparator
Arm Description
Telfa pad dressing placed over Cesarean wound after skin closure; the dressing will be changed to a new Telfa pad dressing on post-operative day 2 which will remain on the incision through post-operative day 7.
Arm Title
Silver-impregnated dressing
Arm Type
Active Comparator
Arm Description
Silver-impregnated dressing placed over Cesarean wound after skin closure; the dressing will be changed to saline-treated dressing on post-operative day 2 which will remain on the incision through post-operative day 7.
Intervention Type
Device
Intervention Name(s)
Silver-impregnated dressing
Other Intervention Name(s)
Silverlon
Intervention Description
Silver-impregnated dressing placed over Cesarean wound after skin closure; the dressing will be changed to saline-treated dressing on post-operative day 2 which will remain on the incision through post-operative day 7.
Intervention Type
Device
Intervention Name(s)
Telfa pad dressing
Other Intervention Name(s)
Telfa pad
Intervention Description
Telfa pad dressing placed over Cesarean wound after skin closure; the dressing will be changed to a new Telfa pad dressing on post-operative day 2 which will remain on the incision through post-operative day 7.
Primary Outcome Measure Information:
Title
Percentage of Patients Who Develop a Surgical Site Infection
Description
A surgical site infection involving the skin and subcutaneous tissue is defined as either The presence of a purulent discharge from the wound on inspection, or Purulent discharge obtained from the wound after exploration based on the suspicion of the provider (erythema, swelling, heat or pain), or The presence of a seroma or hematoma discharge from the wound on inspection or after exploration that also involves isolation of an organism from an aseptically obtained culture based on suspicion of the provider (erythema, swelling, heat or pain). Seromas or hematomas with negative cultures will not be considered a surgical site infection.
Time Frame
from post operative day #1 through post operative day 30
Secondary Outcome Measure Information:
Title
Cosmetic Outcome of the Cesarean Section Incision
Description
The following instruments will be used to determine the cosmetic outcome: • The Modified Vancouver scar scale Range of scale values are from 0-12 (0 indicating a better outcome)
Time Frame
Post operative day 7
Title
Cosmetic Outcome of the Cesarean Section Incision
Description
The following instruments will be used to determine the cosmetic outcome • The Modified Observer Scar Assessment Scale Range of scale values is from 5 - 50 ( the lower the score the better the outcome)
Time Frame
Six weeks post-operative
Other Pre-specified Outcome Measures:
Title
Reduction of Pain After Cesarean Delivery
Description
The amount of narcotics measured in Morphine equivalent milligrams and non opioids administered during the cesarean delivery hospitalization were recorded
Time Frame
Immediately post operatively to hospital discharge
Title
The Number of Participants Noting Pain at the One Week Post Cesarean Visit
Description
Pain response to notable pain at wound site during 7 day post operative visit Subjective self reporting pain as yes or no.
Time Frame
Post operative day 7
Title
The Number of Participants Noting Pain at the Six Weeks Post Cesarean Visit
Description
Pain response to notable pain at wound site during 6 week post operative visit Subjective self reporting of pain as yes or no.
Time Frame
6 weeks post operative

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 or older Elective and emergent cesarean deliveries Primary and repeat cesarean sections Transverse skin incisions (Pfannenstiel) Low transverse uterine incisions Patients with or without the diagnosis of chorioamnionitis with antibiotic treatment prior to or after the delivery of the baby Single and multiple gestations Able and willing to provide written informed consent Exclusion Criteria: Patients that did not receive routine prophylactic dose of antibiotics in the operating room. Skin incisions other than Pfannenstiel Uterine incisions other than low transverse Patients with known or discovered allergy to silver or nylon
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sheila Connery, MD
Organizational Affiliation
USF Health Morsani College of Medicine, Department of Obstetrics and Gynecology
Official's Role
Principal Investigator
Facility Information:
Facility Name
USF Health South Tampa Center for Advanced Healthcare
City
Tampa
State/Province
Florida
ZIP/Postal Code
33606
Country
United States
Facility Name
Women's Center Operating Rooms at the Tampa General Hospital
City
Tampa
State/Province
Florida
ZIP/Postal Code
33606
Country
United States
Facility Name
USF Health Morsani Center for Advanced Healthcare
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
17712651
Citation
Opoien HK, Valbo A, Grinde-Andersen A, Walberg M. Post-cesarean surgical site infections according to CDC standards: rates and risk factors. A prospective cohort study. Acta Obstet Gynecol Scand. 2007;86(9):1097-102. doi: 10.1080/00016340701515225.
Results Reference
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PubMed Identifier
19701037
Citation
Owens SM, Brozanski BS, Meyn LA, Wiesenfeld HC. Antimicrobial prophylaxis for cesarean delivery before skin incision. Obstet Gynecol. 2009 Sep;114(3):573-579. doi: 10.1097/AOG.0b013e3181b490f1.
Results Reference
background
PubMed Identifier
18510455
Citation
Olsen MA, Butler AM, Willers DM, Devkota P, Gross GA, Fraser VJ. Risk factors for surgical site infection after low transverse cesarean section. Infect Control Hosp Epidemiol. 2008 Jun;29(6):477-84; discussion 485-6. doi: 10.1086/587810.
Results Reference
background
PubMed Identifier
17961738
Citation
Epstein NE. Do silver-impregnated dressings limit infections after lumbar laminectomy with instrumented fusion? Surg Neurol. 2007 Nov;68(5):483-5; discussion 485. doi: 10.1016/j.surneu.2007.05.045.
Results Reference
background
Citation
Perkins James, Pattillo Rolandid. How to Avert Postoperative Wound Complications-Treat It when It Occurs. OBG Management 2009;21(10):43-53.
Results Reference
background
PubMed Identifier
18927482
Citation
Huckfeldt R, Redmond C, Mikkelson D, Finley PJ, Lowe C, Robertson J. A clinical trial to investigate the effect of silver nylon dressings on mediastinitis rates in postoperative cardiac sternotomy incisions. Ostomy Wound Manage. 2008 Oct;54(10):36-41.
Results Reference
background
PubMed Identifier
17199764
Citation
Leaper DJ. Silver dressings: their role in wound management. Int Wound J. 2006 Dec;3(4):282-94. doi: 10.1111/j.1742-481X.2006.00265.x.
Results Reference
background
PubMed Identifier
12142678
Citation
Mustoe TA, Cooter RD, Gold MH, Hobbs FD, Ramelet AA, Shakespeare PG, Stella M, Teot L, Wood FM, Ziegler UE; International Advisory Panel on Scar Management. International clinical recommendations on scar management. Plast Reconstr Surg. 2002 Aug;110(2):560-71. doi: 10.1097/00006534-200208000-00031.
Results Reference
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PubMed Identifier
20417924
Citation
Cromi A, Ghezzi F, Gottardi A, Cherubino M, Uccella S, Valdatta L. Cosmetic outcomes of various skin closure methods following cesarean delivery: a randomized trial. Am J Obstet Gynecol. 2010 Jul;203(1):36.e1-8. doi: 10.1016/j.ajog.2010.02.001. Epub 2010 Apr 24.
Results Reference
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PubMed Identifier
15253184
Citation
Draaijers LJ, Tempelman FR, Botman YA, Tuinebreijer WE, Middelkoop E, Kreis RW, van Zuijlen PP. The patient and observer scar assessment scale: a reliable and feasible tool for scar evaluation. Plast Reconstr Surg. 2004 Jun;113(7):1960-5; discussion 1966-7. doi: 10.1097/01.prs.0000122207.28773.56.
Results Reference
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Citation
Thomas Steve. MRSA and the Use of Silver Dressings: Overcoming Bacterial Resistance. http://www.worldwidewounds.com/2004/november/Thomas/Introducing-Silver Dressings.html.
Results Reference
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Citation
Yiannias, James. Clinical features and diagnosis of allergic contact dermatitis. http://www.uptodate.com/contents/clinical-features-and-diagnosis-of-allergic-contact-dermatitis
Results Reference
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PubMed Identifier
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Citation
Connery SA, Yankowitz J, Odibo L, Raitano O, Nikolic-Dorschel D, Louis JM. Effect of using silver nylon dressings to prevent superficial surgical site infection after cesarean delivery: a randomized clinical trial. Am J Obstet Gynecol. 2019 Jul;221(1):57.e1-57.e7. doi: 10.1016/j.ajog.2019.02.053. Epub 2019 Mar 5.
Results Reference
derived

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Prospective Study on Cesarean Wound Outcomes

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