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Prospective observational study of preoperative complete colorectal evaluation after colorectal stent placement for obstructive colorectal cancer.

Prospective observational study of preoperative complete colorectal evaluation after colorectal stent placement for obstructive colorectal cancer. - Prospective observational study of preoperative complete colorectal evaluation after colorectal stent placement for obstructive colorectal cancer.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000040911
Enrollment
30
Registered
2020-07-01
Start date
2020-07-01
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

obstructive colorectal cancer

Interventions

None listed

Sponsors

Department of Gastroenterology, Japanese Red Cross Okayama Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients who underwent colorectal stent placement for resectable colorectal cancer with stenosis. 2. Provided written informed consent.

Exclusion criteria

Exclusion criteria: 1. Severe complication 2. Within 2 days until surgery after colorectal stent placement 3. Inappropriate cases by investigators

Design outcomes

Primary

MeasureTime frame
Detection rate of synchronous colon cancers on the oral side of stenosis

Secondary

MeasureTime frame
1.Success rate of complete colonoscopy after colorectal stent placement 2.Complication rate of complete colonoscopy after colorectal stent placement 3.Risk factor of unsuccessful complete colonoscopy after colorectal stent placement 4.Detection rate of neoplastic lesions on the oral side of stenosis using complete colonoscopy 5.Detection rate of neoplastic lesions on the oral side of stenosis using CT colonography

Countries

Japan

Contacts

Public ContactYutaka Akimoto

Japanese Red Cross Okayama Hospital Department of Gastroenterology

qttsp974@gmail.com086-222-8811

Outcome results

None listed

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