Trials / Completed
CompletedNCT02916511
Study of Extensive Clinical Target Volumes in Postoperative Radiotherapy Concurrent With Chemotherapy for Esophageal Squamous Cell Carcinoma
- Status
- Completed
- 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 extensive clinical target volumes in postoperative radiotherapy concurrent with chemotherapy for esophageal squamous cell carcinoma.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Paclitaxel | paclitaxel 50mg/m2/d, ivgtt over 3 hours, d1, qw\*5 |
| DRUG | Carboplatin | carboplatin AUC=2, ivgtt, d1, qw\*5 |
| RADIATION | Radiotherapy | 1.8Gy/d, d1-5/week, 25Fx |
Timeline
- Start date
- 2016-09-01
- Primary completion
- 2021-07-01
- Completion
- 2023-07-01
- First posted
- 2016-09-27
- Last updated
- 2023-12-22
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT02916511. Inclusion in this directory is not an endorsement.