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To determine efficacy of using 3 minutes povidone-soaked suture in reducing surgical site infection during wound closure in elective surgery.
Participant recruitment and randomisation based on eligibility based on CONSORT.
Patient will get either package A or B which determine whether they are getting povidone-soaked suture or ordinary suture during wound closure.
Postoperative, follow up on D10 and D30 of patient well being and signs and symptoms of surgical site infection
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| povidone-soaked suture | Experimental | The patient is randomized, those with povidone-soaked suture group will be prepared for povidone-soaked suture during wound closure. The absorbable suture will be soaked into povidone for 3 mins before the wound closure. |
|
| ordinary suture | Active Comparator | the patient is randomized, those with ordinary suture group will proceed with wound closure as usual manner following the standard practice. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| povidone-soaked suture | Other | suture soak with povidone solution for 3 mins |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Povidone-soaked Sutures versus Ordinary Sutures for Reducing Surgical Site Infection: Randomize Control Trial Study in General Surgery Cases of Hospital Universiti Sains Malaysia | There is difference of outcome using povidone-soaked suture and ordinary suture. In this study, our hypothesis the suture with povidone-soaked will reduce the SSIs rate during closure and it will be assessed on day 10 and day 30 post-operative. Few measurement are used in detection of SSI based on clinical and biochemical measurement such as signs of inflammation and total white cell count. | 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| Povidone-soaked Sutures versus Ordinary Sutures for Reducing Surgical Site Infection: Randomize Control Trial Study in General Surgery Cases of Hospital Universiti Sains Malaysia | There is association between povidone-soaked suture and ordinary suture in reducing surgical site infection. There is difference of outcome using povidone-soaked suture and ordinary suture. In this study, our hypothesis the suture with povidone-soaked will reduce the SSIs rate during closure and it will be assessed on day 10 and day 30 post-operative. Few measurement are used in detection of SSI based on clinical and biochemical measurement such as signs of inflammation and total white cell count. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| SITI HAFZAN ABD KARIM, MD | UNIVERSITI SAINS MALAYSIA- HEALTH CAMPUS | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Universiti Sains Malaysia | Kubang Kerian | Kelantan | 16150 | Malaysia |
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| ID | Term |
|---|---|
| D013530 | Surgical Wound Infection |
| ID | Term |
|---|---|
| D014946 | Wound Infection |
| D007239 | Infections |
| D011183 | Postoperative Complications |
| D010335 | Pathologic Processes |
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randomized control trial, double blind
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| ordinary suture |
| Other |
suture no need to soak with povidone solution |
|
| 6 months |
| Povidone-soaked Sutures versus Ordinary Sutures for Reducing Surgical Site Infection: Randomize Control Trial Study in General Surgery Cases of Hospital Universiti Sains Malaysia | There is difference in the extent of intervention needed to manage SSIs in wounds closed with povidone-soaked suture and ordinary suture. This hypothesis measure how far that the management of SSIs whether non-operative or operative treatment is needed. This is base on antibiotic use, dressing and surgical intervention such as debridement. | 6 months |
| D013568 |
| Pathological Conditions, Signs and Symptoms |