CI

At a glance

ClinicalIndex Comparison Record
Phase 3Recruiting· 266 target
Drug / intervention
Cisplatin +2 moredrug
Likely dose
Cisplatin 100 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04436965
NCT04436965Phase 3RecruitingOn Track
Long Recruiting

Effect of Standard Nutrition Therapy on Nutritional Status and Prognosis in Locoregionally Advanced Nasopharyngeal Carcinoma Patients With Malnutrition: A Prospective, Multicenter, Phase III Randomized Control Clinical Trial

Sun Yat-sen University·interventional·Posted Jun 18, 2020·Updated May 11, 2026

In Brief

A Phase 3 clinical trial evaluating Standardized nutrition therapy, Cisplatin, and 1 other intervention for Nasopharyngeal Carcinoma and Nutrition Therapy. Currently recruiting, targeting 266 participants across 1 site.

Detailed Summary

This is a multicenter, randomized controlled, phase III clinical trial. The purpose of this study is to evaluate the efficacy of standard nutrition treatment versus conventional nutrition treatment in local advanced nasopharyngeal carcinoma patients.

Study Details

Timeline

Phase 3Recruiting
2021202220232024202520262027202820292030
First PostedJun 18, 2020
Enrollment StartAug 16, 2021
Primary CompletionDec 1, 2026
Study CompletionDec 1, 2029
TodayJul 1, 2026
Enrollment to primary: 5.3 yearsPosted 6.0 years agoPrimary completion in 5 months

Interventions

Standardized nutrition therapyother

Standardized nutrition therapy with ONS, nasal feeding tube, PEG or parenteral nutrition

Cisplatindrug

Patients in both arms received concurrent cisplatin chemotherapy:100 mg/m² cisplatin given intravenously every 3 weeks on days 1, 22 concurrently with radiotherapy.

Intensity Modulated Radiation Therapyradiation

Patients in both arms received Intensity Modulated Radiation Therapy:All target volumes were outlined slice by slice on the axial contrast-enhanced CT with MR fusion images in the treatment planning system. The target volumes were defined in accordance with the International Commission on Radiation Units and Measurements Reports 83. The prescribed dose was 70-72 Gy to PTVnx (Planning target volume of the primary tumor), 64-70 Gy to PTVnd (Planning target volume of the cervical lymph node),60- 64Gy to PTV1 (Planning target volume 1), and 54-58 Gy to PTV2 (Planning target volume 2) in 30-32 fractions. The details of dose limits for organs at risk were based on the study 0225 from The Radiation Therapy Oncology Group (RTOG 0225).