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A randomized controlled phase II/III study comparing EBD combined with steroid to RIC combined with steroid for refractory anastomotic stricture after esophagectomy (JCOG1207: RICS study)

Phase 2
Recruiting
Conditions
Refractory anastomotic stricture after surgical resection for esophageal cancer
Registration Number
JPRN-UMIN000014017
Lead Sponsor
Japan Clinical Oncology Group (JCOG)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
130
Inclusion Criteria

Not provided

Exclusion Criteria

1) Active infection requiring systemic therapy 2) Body temperature >=38 degrees Celsius 3) Pregnancy, possible pregnancy within 28 days after delivery or breastfeeding 4) Psychiatric disease 5) Patients requiring systemic steroid medication 6) Patients requiring continuous anticoagulant or antiplatelet drug 7) Poorly controlled hypertension 8) Unstable angina within 3 weeks, or with a history of myocardial infarction within 6 months

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Phase II: Proportion of Grade 3/4 intraoperative hemorrhage, esophageal perforation or hemorrhage, pneumothorax, lung or mediastinum infection, or other unexpected adverse reactions. Phase III: Restenosis-free survival; Number of dilation for 24 weeks after treatment
Secondary Outcome Measures
NameTimeMethod
Phase II/III: Proportion of patients with anastomotic diameter > 10 mm at the time of 8 weeks after treatment; Proportion of adverse events; Proportion of patients experiencing improvement of dysphagia score at the time of 2, 4, 8, 24 weeks after treatment; Proportion of patients with dysphagia score <= 1 at the time of 24 weeks after treatment.
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