Surgery Alone Verus Sugery Combined with Dose-reduced Radiotherapy for Newly Diagnosed Stage I Nasopharyngeal Carcinoma

NCT06688760 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 86

Last updated 2024-11-14

No results posted yet for this study

Summary

The goal of this clinical trial is to compare the efficacy and safety of endoscopic nasopharyngectomy combined with retropharyngeal lymph nodes dissection plus bilateral upper neck lymph node dissection or plus postoperative low-dose radiotherapy in newly diagnosed stage Ⅰ nasopharyngeal carcinoma.

Conditions

  • Nasopharyngeal Carcinoma
  • Surgery
  • Radiotherapy

Interventions

PROCEDURE

Endoscopic nasopharyngectomy combine Retropharyngeal lymphadenectomy and Low Dose Radiotherapy

in experimental arm 1

PROCEDURE

Endoscopic nasopharyngectomy combine Retropharyngeal lymphadenectomy and Double upper neck lymph node dissection

in experimental arm 2

Sponsors & Collaborators

  • Fifth Affiliated Hospital, Sun Yat-Sen University

    collaborator OTHER
  • Sun Yat-sen University

    collaborator OTHER
  • Fifth Affiliated Hospital of Guangzhou Medical University

    collaborator OTHER
  • Huazhong University of Science and Technology Union Hospital (Nanshan Hospital)

    collaborator UNKNOWN
  • Nanfang Hospital, Southern Medical University

    collaborator OTHER
  • First Affiliated Hospital, Sun Yat-Sen University

    collaborator OTHER
  • First People's Hospital of Foshan

    collaborator OTHER
  • Zhongshan People's Hospital, Guangdong, China

    collaborator OTHER
  • Ming-Yuan Chen

    lead OTHER

Principal Investigators

  • Ming-Yuan Chen, MD,PhD · SUN yet-sen 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
2023-11-01
Primary Completion
2028-11-01
Completion
2028-11-01

Countries

  • China

Study Locations

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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 NCT06688760 on ClinicalTrials.gov