Clinical trial for deep-cavity wound dressings to evaluate the effectiveness and safety of anti-adhesion after ileostomy

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002513

Enrollment

Registered

2017-10-27

Start date

2017-03-06

Completion date

Unknown

Last updated

2019-03-11

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

Conditions

None listed

Interventions

Medical Device : Those who have been diagnosed as needing to perform ileus repair after incisional opening through the incision will be referred to this trial. If there is no adherence and the final n

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: ? Adult male or female over 19 years of age ? Those who are scheduled to undergo reconstruction after reconstruction of the ileum ? Those who are reliable and willing to cooperate in this test, and obey the restrictions for the treatment period

Exclusion criteria

Exclusion criteria: ? Pregnant or lactating women, pregnant women with a pregnancy plan ? If you have had laparotomy with incision or have a history of adhesion around the incision site ? Peritoneal infection, intraabdominal infection such as intraabdominal abscess ? Patients who continued to receive Corticosteroids 20 mg / day or more within 30 days before surgery ? If you have blood clotting dysfunction ? If the immune function is decreased ? When researchers evaluate that it is not appropriate to participate in this clinical test

Design outcomes

Primary

Measure	Time frame
Primary efficacy outcome: incidence of adhesions in the pelvic floor area during ileus repair (%)	—

Secondary

Measure	Time frame
Adverse event	—

Countries

Korea, Republic of

Contacts

Public ContactHani Lee

Samsung Medical Center

hani0831.lee@samsung.com+82-2-3410-1655

Outcome results