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Short term outcomes of Randomized Controlled Trial of Senhance Digital Laparoscopy System versus Laparoscopic colectomy for colon cancer

Short term outcomes of Randomized Controlled Trial of Senhance Digital Laparoscopy System versus Laparoscopic colectomy for colon cancer - Short term outcomes of Randomized Controlled Trial of Senhance Digital Laparoscopy System versus Laparoscopic colectomy for colon cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000053839
Enrollment
200
Registered
2024-03-16
Start date
2025-01-01
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

colon cancer

Interventions

Senhance digital laparoscopy system Laparoscopic surgery

Sponsors

Saitama medical university international medical center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Cases with Informed Consent Clinical stage 0-3 adenocarcinoma Radical surgery is planned Tumor site in cecum, ascending colon, sigmoid colon, or sigmoid rectum Tumor length 4-0 cm or less Patient age 20-80 years Performance status ECOG 0-1. No previous gastrointestinal surgery other than appendectomy No organ dysfunction or hematologic abnormality

Exclusion criteria

Exclusion criteria: Multiple cancers Active infectious disease Previous psychiatric and/or central nervous system disorders Pregnancy, lactation, or possible pregnancy Serious concomitant illness (cardiopulmonary dysfunction, renal failure, intestinal paralysis, intestinal obstruction, uncontrolled disease, etc.) (intestinal paralysis, intestinal obstruction, uncontrolled diabetes, renal failure, cirrhosis, chronic hepatitis B, chronic hepatitis C, etc.) No history of organ transplantation Receiving preoperative treatment for colorectal cancer (chemotherapy, radiation therapy, hormonal therapy, etc.) Patients deemed unsuitable for study enrollment by the investigator

Design outcomes

Primary

MeasureTime frame
Postoperative complications

Secondary

MeasureTime frame
Operarive times, blood loss, intraoperative complications, conversion rate, postoperative stays, pathlogical findings

Countries

Japan

Contacts

Public ContactYasuhiro Ishiyama

Saitama medical university international medical center Gastroenterological surgery

cesarishimar1215@yahoo.co.jp0429844111

Outcome results

None listed

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