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A phase II study of percutaneous trans-esophageal gastric tubing for malignant gastrointestinal obstruction (JIVROSG-0205)

A phase II study of percutaneous trans-esophageal gastric tubing for malignant gastrointestinal obstruction (JIVROSG-0205) - Percutaneous trans-esophageal gastric tubing (JIVROSG-0205)

Status
Unknown
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-C000000249
Enrollment
33
Registered
2006-09-01
Start date
2003-07-01
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

Malignant gastrointestinal obstruction

Interventions

Sponsors

Japan Interventional Radiology in Oncology Study Group (JIVROSG)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) No expectation for removal of nasal tube caused by persistent and malignant gastro-intestinal obstruction. 2) No pathological condition around cervical esophagus. 3) Adequate cardiac, hepatic, renal, respiratory, and bone marrow functions. 4) Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 3. 5) Expected survival more than 4 weeks. 6) Written informed consent.

Exclusion criteria

Exclusion criteria: 1) Tracheostomy. 2) Intestinal obstruction due to the lesions between transverse colon and rectum. 3) Pregnancy. 4) Local therapy for neck region

Design outcomes

Primary

MeasureTime frame
Improvement of subjective symptoms compared to previous nasal tubing.

Secondary

MeasureTime frame
Adverse events and feasibility of procedure

Countries

Japan

Contacts

Public ContactYasuaki Arai

JIVROSG, Coordinating Office Division of Diagnostic Radiology, National Cancer Center Hospital

jvrosgffice@ml.res.ncc.go.jp0335422511

Outcome results

None listed

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