A Trial Estimating The Optimal Radiation Volume Of Postsurgical Radiation For Patients With Esophageal Cancer

NCT01391572 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2011-07-22

No results posted yet for this study

Summary

A randomized phase II trial to estimate the optimal radiation volume of postsurgical radiation for patients with locoregionally advanced thoracic esophageal squamous cell carcinoma (T3-4, any N, M0).

Conditions

Interventions

RADIATION

enlarge irradiation volume

In Arm A, postsurgical radiation target volume includes tumor bed and elective nodes area

RADIATION

Small volume radiation

In Arm B, postsurgical radiation target volume includes tumor bed only

DRUG

cisplatin

Sponsors & Collaborators

  • The First Affiliated Hospital of Soochow University

    collaborator OTHER
  • The Affiliated Tumor Hospital of Nantong University, Nantong, Jiangsu Province, China

    collaborator OTHER
  • Jiangsu Cancer Institute & Hospital

    collaborator OTHER
  • Affiliated Hospital of Jiangsu University

    collaborator OTHER
  • Zhejiang Cancer Hospital

    collaborator OTHER
  • First Affiliated Hospital of Wenzhou Medical University

    collaborator OTHER
  • Zhejiang University

    collaborator OTHER
  • The First Affiliated Hospital of Anhui Medical University

    collaborator OTHER
  • Anhui Provincial Hospital

    collaborator OTHER_GOV
  • Fujian Cancer Hospital

    collaborator OTHER_GOV
  • Shanghai Chest Hospital

    collaborator OTHER
  • Shanghai Pulmonary Hospital, Shanghai, China

    collaborator OTHER
  • RenJi Hospital

    collaborator OTHER
  • Fudan University

    lead OTHER

Principal Investigators

  • Xiao-Long Fu, M.D, Ph.D. · Fudan University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-04-30
Primary Completion
2013-12-31

Countries

  • China

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01391572 on ClinicalTrials.gov