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Effectiveness of Glove Changing in Reducing Wound-related Complications

Primary Purpose

Wound Complication

Status
Completed
Phase
Not Applicable
Locations
Vietnam
Study Type
Interventional
Intervention
glove changing
Sponsored by
Hung Vuong Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Wound Complication focused on measuring Complications, Glove changing, Eesarean surgery, Infections, Vietnam

Eligibility Criteria

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

Inclusion criteria pregnant women were 18 years old or higher; pregnant women had cesarean surgery performed at Hung Vuong hospital; pregnant women lived close to Ho Chi Minh city and agreed to return for postpartum care one-month post-surgery. Exclusion criteria pregnant women had fever during labor; pregnant women had systemic infectious conditions; pregnant women had surgical site infection SSI or sexually infectious conditions; pregnant women had ongoing internal conditions such as pre-eclampsia, severe anemia, American Society of Anesthesiologists (ASA) ≥ 3, New York Heart Association (NYHA) class 3 or above, pulmonary edema, or severe asthma.

Sites / Locations

  • Hung Vuong hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Glove change group

Usual care group

Arm Description

The surgical gloves were changed prior to closure of the peritoneum or closure of the abdominal fascia

The surgical gloves were not changed before abdominal closure

Outcomes

Primary Outcome Measures

Wound complications
Seroma, hematoma, wound separation, and wound infection

Secondary Outcome Measures

Surgical site infection
Fever, swelling, redness, and pain surrounding the incisional area

Full Information

First Posted
February 18, 2023
Last Updated
February 28, 2023
Sponsor
Hung Vuong Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05748743
Brief Title
Effectiveness of Glove Changing in Reducing Wound-related Complications
Official Title
Using a Randomized Control Trial to Evaluate the Effectiveness of Glove Changing in Reducing Wound-related Complications Following Cesarean Section in Vietnam
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
December 18, 2020 (Actual)
Primary Completion Date
February 25, 2021 (Actual)
Study Completion Date
February 25, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hung Vuong 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
This study aimed to investigate the effectiveness of glove changing in reducing complications of cesarean deliveries in Vietnam.
Detailed Description
In Vietnam, the rate of Cesarean section (CS) is very high, ranging from 40-50%. Despite that, there are very limited publications concerning the risk factors, complications, and management of surgical site infection (SSI) following CS. Our study is the first to investigate the effectiveness of glove changing in reducing the incidence of post-operative infections in Vietnam. Specifically, the aims of this study are 1) to evaluate whether changing gloves during CS reduces complications and SSI, and 2) to identify other factors that are associated with complications and SSI.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Wound Complication
Keywords
Complications, Glove changing, Eesarean surgery, Infections, Vietnam

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study is a parallel-group randomized control trial with 2 arms. Arm 1 includes patients who will have glove changed prior to abdominal closure during cesarean surgery. Aim 2 includes patients who will not have glove changed prior to abdominal closure during cesarean surgery. All patients are randomized using computer-generated sequences with allocation ratio 1:1. Clinic visits are performed at 2 time points. Visit 1 is at 2-3 days post-surgery and visit 2 is at 30 ± 2 days post-surgery where primary and secondary outcomes are measured. The primary outcomes of interest are any wound complications occurring after the surgery, including seroma, hematoma, wound separation, and wound infection. Secondary outcomes are any signs of SSI, including fever, swelling, redness, and pain surrounding the incisional area. The outcomes will be evaluated during clinic visits by qualified medical practitioners who are blind to the intervention group assignment.
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
Participants, investigators, and outcomes assessor are blind to the intervention group assignment.The only people that were unmasked were the surgical team.
Allocation
Randomized
Enrollment
678 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Glove change group
Arm Type
Experimental
Arm Description
The surgical gloves were changed prior to closure of the peritoneum or closure of the abdominal fascia
Arm Title
Usual care group
Arm Type
No Intervention
Arm Description
The surgical gloves were not changed before abdominal closure
Intervention Type
Procedure
Intervention Name(s)
glove changing
Intervention Description
Surgical gloves were changed prior to abdominal closure during Cesarean section to evaluate its effectiveness in reducing wound complications after surgery
Primary Outcome Measure Information:
Title
Wound complications
Description
Seroma, hematoma, wound separation, and wound infection
Time Frame
Within 4 weeks after surgery
Secondary Outcome Measure Information:
Title
Surgical site infection
Description
Fever, swelling, redness, and pain surrounding the incisional area
Time Frame
Within 4 weeks after surgery

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
We only recruited pregnant women to participate in this study
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria pregnant women were 18 years old or higher; pregnant women had cesarean surgery performed at Hung Vuong hospital; pregnant women lived close to Ho Chi Minh city and agreed to return for postpartum care one-month post-surgery. Exclusion criteria pregnant women had fever during labor; pregnant women had systemic infectious conditions; pregnant women had surgical site infection SSI or sexually infectious conditions; pregnant women had ongoing internal conditions such as pre-eclampsia, severe anemia, American Society of Anesthesiologists (ASA) ≥ 3, New York Heart Association (NYHA) class 3 or above, pulmonary edema, or severe asthma.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tuyet Hoang, Doctor
Organizational Affiliation
Hung Vuong Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Hung Vuong hospital
City
Ho Chi Minh City
Country
Vietnam

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Effectiveness of Glove Changing in Reducing Wound-related Complications

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