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Development of predictive and preventive methods for post-esophageal ESD stricture

Development of predictive and preventive methods for post-esophageal ESD stricture - Clinical predictor and prevention of esophageal stricture

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000031985
Enrollment
74
Registered
2018-04-15
Start date
2018-03-28
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

superficial esophageal neoplasms

Interventions

A: After local steroid (triamcinolone acetonide 100 mg) injection to the ulcer, prednisolone is started on post-operative day 3 at a dose of 30 mg/day. The administration of steroids was discontinued

Sponsors

Division of Gastroenterology and Hematology/Oncology, Department of Medicine, Asahikawa Medical University
Lead Sponsor
Asahikawa-Kosei General Hospital Asahikawa City hospital Japanese Red Cross Asahikawa Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patients over 20 years of age 2)Patients who are histologically proven esophageal squamous cell carcinoma or intraepithelial neoplasia 3)Patients with primary tumor located in the epithelium, lamina propria mucosa, muscularis mucosa or submucosa confirmed by endoscopy 4)Patients with dysphagia score of 0 5)Patients who admit to a hospital 6)Patients with written informed consent.

Exclusion criteria

Exclusion criteria: 1)Patients with prior radiotherapy to the neck, chest wall, lung, or mediastinum 2)Patients with primary tumor located within 20mm from prior EMR/ESD treatment site 3)Patients who fail to pass through the prior EMR/ESD treatment site by a standard endoscope (for the upper gastrointestinal tract) 4)Patients with surgery or radiotherapy for esophagus within 3 months after esophageal ESD 5)Patients who judged inappropriate by an attendant physician

Design outcomes

Primary

MeasureTime frame
stricture-free survival

Secondary

MeasureTime frame
the number of endoscopic balloon dilation for 12 weeks after ESD, adverse events and proportion of patients with dysphagia score=<1 at the time of 12 weeks after ESD

Countries

Japan

Contacts

Public ContactKeitaro Takahashi

Asahikawa Medical University Division of Gastroenterology and Hematology/Oncology, Department of Medicine

ktakaha@asahikawa-med.ac.jp0166-68-2462

Outcome results

None listed

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