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Active Not RecruitingNCT04764227

Phase II Study of Postoperative Concurrent Chemoradiotherapy for Esophageal Squamous Cell Carcinoma (ESO- Shanghai 17)

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
70 (actual)
Sponsor
Fudan University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate safety and 2-year local control rate for postoperative concurrent chemoradiotherapy for esophageal squamous cell carcinoma.

Conditions

Interventions

TypeNameDescription
DRUGPaclitaxelpaclitaxel 50mg/m2/d, ivgtt over 3 hours, d1, qw\*5
DRUGCarboplatincarboplatin AUC=2, ivgtt, d1, qw\*5
RADIATIONRadiotherapy1.8Gy/d, d1-5/week, 28Fx

Timeline

Start date
2020-05-30
Primary completion
2024-03-30
Completion
2027-03-30
First posted
2021-02-21
Last updated
2023-08-03

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04764227. Inclusion in this directory is not an endorsement.