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Prospective randomized controlled study about the adhesion prevention safety and effects for the general surgery using the absorbable adhesion barrier (INTERCEED) made of oxidized regenerated cellulose.

Prospective randomized controlled study about the adhesion prevention safety and effects for the general surgery using the absorbable adhesion barrier (INTERCEED) made of oxidized regenerated cellulose. - Randomized controlled trials of the safety and effectiveness of the anti-adhesion for the abdominal surgery using the synthetic absorbable adhension barrier.(SAAB)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000010314
Enrollment
100
Registered
2013-03-25
Start date
2013-04-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

colorectal cancer

Interventions

A piece of dried interceed which is 3-5mm larger than the surgery site will be placed to prevent adhesion just before abdominal closure of the laparoscopic surgery. Normal laparoscopic surgery (withou

Sponsors

Kitasato University Department of Surgery
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who aged over 20 years old Patients who adapt for the laparoscopic surgery of the lower gastrointestinal Patients who have intention of the participation in this study and agree to sign on the written informed consent Patients who are judged as appropriate using interceed by a doctor

Exclusion criteria

Exclusion criteria: Patients who have persistence of cancer macroscopically Patients who are given anticancer drugs intraperitoneally Patients who have sever hapatic damage, kidney damage, heart disease and infection desease Patients who will be used other anti-adhesion methods in both groups including the non-use interceed Patients who will be used over the site that has been soaked in blood Patients who will be used over the contaminated or infected wound Patients who have history of severe drug allergy Patients who have history of oxidized regenerated cellulose allergy Patients who are judged inappropriate by a doctor

Design outcomes

Primary

MeasureTime frame
Frequency of serious adverse event within 30 days from surgery.

Secondary

MeasureTime frame
Frequency of serious adverse event within 6 months after surgery. Frequency of infection of the surgical site within 30 days and 6 months after surgery. Frequency of adhesive ileus within 30 days and 6 months after surgery. The use of evaluation of the intercede during surgery.

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026