Prospective Feasibility Study of D-Weave Uncovered Stent for Colon Protocol

Prospective Feasibility Study of D-Weave Uncovered Stent for Colon Protocol - Colonic D-Weave Stent Protocol

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000011304

Enrollment

200

Registered

2013-07-29

Start date

2013-10-01

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

malignant colo-rectal strictures

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients requiring palliative treatment of colorectal strictures produced by malignant neoplasms. Only patients with no previous colonic stenting will be included in the registry.

Exclusion criteria

Exclusion criteria: Patients contraindicated will include those presenting - enteral ischemia - benign stricture - suspected or impending perforation - intrabdominal abscess / perforation - strictures that do not allow passage of a guide wire - patients for whom endoscopic techniques are contraindicated - any use other than those specifically outlined under indications of use (inclusion)

Design outcomes

Primary

Measure	Time frame
Clinical Efficacy of Colonic D-Weave Uncovered Stent, associated to Obstruction Relief and Permeability	—

Secondary

Measure	Time frame
Additional data related to the procedure and the product: Technical success, Complications, Survival, Palliation vs Bridge to Surgery	—

Countries

Japan

Contacts

Public ContactToshiyuki Enomoto

Toho University Ohashi Medical Center Surgery

eno@med.toho-u.ac.jp03-3468-1251

Outcome results