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ADOBARRIER study

A multicenter randomized controlled trial of the multifaceted work load reduction of anti-adhesion barrier for diverting ileostomy in laparoscopic rectal surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs032200155
Enrollment
120
Registered
2020-10-15
Start date
2020-12-02
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

Rectal cancer

Interventions

randomized controlled trial

Sponsors

Watanabe Jun
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patient selection criteria Patients who meet all of the following eligibility criteria 1. Age at the time of registration is 20 years or older. 2. Patients diagnosed with rectal cancer (including NET). 3. Patients scheduled for laparoscopic rectal resection. 4. Patients scheduled for temporary ileal colostomy. 5. Patients scheduled for colostomy within 6 to 48 weeks after surgery. 6. Patients who have the judgment to fully understand the research content. 7. Patients with written informed consent to participate in this study. Operator selection criteria An operator who meets the following criteria 1.Primary surgeon of temporary colostomy.

Exclusion criteria

Exclusion criteria: Patient exclusion criteria Patients who do not violate the following exclusion criteria 1. Patients scheduled for temporary colostomy in the transverse colon. 2. Patients scheduled to undergo open surgery. 3. Minors or patients who are judged not to have sufficient judgment to understand the content of this study. 4. Patients who are pregnant, may be pregnant, or wish to become pregnant during the treatment period. 5. Other patients who are judged to be unsuitable as a subject by the doctor's judgment. Operator exclusion criteria An operator who meets the following criteria 1.An operator who has less than 5 experience as an operator for closure of ileostomy.

Design outcomes

Primary

MeasureTime frame
Multifaceted workload of the primary operator (value of SURG TLX).

Secondary

MeasureTime frame
Operative time and blood loss for closure of ileostomy Evaluation of adhesions during closure of ileostomy State of intestinal dissection during closure of ileostomy

Contacts

Public ContactYusuke Suwa

Yokohama City University Medical Center

ysuwa@yokohama-cu.ac.jp+81-45-261-5656

Outcome results

None listed

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