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The Effects of Wound Protector to Decrease the Surgical Site Infection in Open Abdominal Surgery, Double-Blind Prospective Randomized Controlled Trial

The Effects of Wound Protector to Decrease the Surgical Site Infection in Open Abdominal Surgery, Double-Blind Prospective Randomized Controlled Trial.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20180508002
Enrollment
Unknown
Registered
2018-05-08
Start date
2016-09-01
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Focus on the patient who undergone laparotomy. Intra&#45

Interventions

Using of Double&#45
O&#45
wound protector in laparotomy procedure,Conventional retractor when surgery
Experimental Device,No Intervention Device
Wound protector group,Non&#45
Wound protector group

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: The patient who have indications for laparotomy surgery Age between 18-80 years

Exclusion criteria

Exclusion criteria: The patients who need re-operation Immunocompromised patients The patients recieving chemotherapy The patients recieving abdominal radiation Pregnancy The ASA classification more than 3 The patients who did not close the skin as primary closure.

Design outcomes

Primary

MeasureTime frame
Surgical site infection Everyday in hospital and 30 days after surgery CDC criteria for diagnosis of surgical site infection—

Secondary

MeasureTime frame
N/A N/A N/A—

Countries

Thailand

Contacts

Public ContactPhongthorn Tuntivararut

Police general hospital

phongthorn007@hotmail.com0816131669

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026