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A confirmatory study of TRM-270 in comparison with Seprafilm in patients with rectal cancer receiving surgery

A confirmatory study to investigate efficacy, safety and handling of TRM-270 in comparison with Seprafilm in patients with rectal cancer receiving laparoscopic or robotic-assisted surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2032220451
Enrollment
260
Registered
2022-11-21
Start date
2022-11-28
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

When performing primary tumor resection and temporary loop ileostomy, subjects will have 4 sheets of TRM-270 (quarter size) or Seprafilm (quarter size), which are anti-adhesion absorption barriers, ap

Sponsors

Tomita Shinpei
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Patients aged between 18 and 80 at the time of informed consent - Patients with initial and primary rectal cancer - Patients with cStage 0 to cStage III - Patients scheduled to undergo laparoscopic or robot-assisted primary tumor resection and temporary loop ileostomy - Patients scheduled for stoma site marking - Patients scheduled to undergo the closure of ileostomy 8 to 52 weeks after initial surgery. - Patients with an ECOG Performance Status of 0 to 1

Exclusion criteria

Exclusion criteria: - Patients considered less than one year of life expectancy based on the course of their disease - Patients with a BMI of 30 or higher - Patients with any of the following complications: a. Peritonitis b. Abscess in the abdominal or pelvic cavity c. Obstructive enteritis or intestinal obstruction d. Infection requiring systemic treatment e. Active double cancer f. Disease requiring laparotomy during the study period g. Severe diabetes or impaired glucose metabolism h. Hypersensitivity to components of TRM-270 including metabolites such as polyethylene glycol or to Seprafilm - Patients with any of the following history: a. Intra-abdominal or pelvic surgery except appendicitis surgery b. Intra-abdominal or pelvic radiotherapy performed at least 1 year before informed consent c. Anti-VEGF antibody or anti-EGFR antibody treatment d. Peritonitis - Patients receiving any of the following treatments: a. Continuous systemic administration of steroids b. Treatment targeting cytokines - Female patients who are pregnant, breastfeeding, have a positive pregnancy test before enrollment, or wish to become pregnant during the study period

Design outcomes

Primary

MeasureTime frame
Occurrence rate of adhesion in small incisions

Contacts

Public ContactShinpei Tomita

ASKA Pharmaceutical Co., Ltd.

aska-clinical@aska-pharma.co.jp+81-80-6645-9201

Outcome results

None listed

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