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Application of Whole-course Standardized Nutrition Management During Peri-radiotherapy in Patients With Nasopharyngeal Carcinoma After Radiotherapy: a Multicenter Randomized Controlled Clinical Study

Application of Whole-course Standardized Nutrition Management During Peri-radiotherapy in Patients With Nasopharyngeal Carcinoma After Radiotherapy: a Multicenter Randomized Controlled Clinical Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05008471
Enrollment
388
Registered
2021-08-17
Start date
2021-04-26
Completion date
2022-04-26
Last updated
2021-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nasopharyngeal Carcinoma, Nutrition Disorders, Radiation Therapy Induced Change

Brief summary

This study will present an advanced equipment of tumor nutrition diagnosis and assesment for nasopharyngeal cancer(NPC) radiotherapy patients in nutritional risk screening, evaluation, diagnosis and directing nutritional intervention, aiming to explore the advantages of the whole nutritional management in acute radiation reaction rate, completion rate of radiotherapy, nutritional status, and quality of life for NPC patients.

Detailed description

In this study, nutrition intervention was performed in one group of nasopharyngeal carcinoma patients with no nutritional risk during the periperiod of radiotherapy , and the other group with no additional intervention when without nutritional risks, for evaluating the value of overall nutritional management in the periperiod radiotherapy.

Interventions

DIETARY_SUPPLEMENTFormula nutrition

The target energy of radiotherapy patients is recommended to be 25-30kcal/(kg·d), and the target energy of the intervention group should be increased by an additional 50% daily from the beginning of radiotherapy. Specifically, under the condition of ensuring the daily target energy 14kcal/(kg·d), formula nutrition should be added daily.

Sponsors

First Affiliated Hospital, Sun Yat-Sen University
CollaboratorOTHER
Second Affiliated Hospital, Sun Yat-Sen University
CollaboratorOTHER
Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with nasopharyngeal carcinoma confirmed by histopathology * Newly diagnosed patients without distant metastasis * Age \>18 * KPS ≥ 70 * Nasopharyngeal radiotherapy alone or concurrent chemoradiotherapy was planned to be received, andIMRT was used for radiotherapy * The patient's blood counts,the lung, liver and renal functions were tolerant to radiotherapy/chemoradiotherapy( WBC ≥ 4.0\*109/L, NE ≥ 2.0\*109/L, PLT 100\*109/L and Hb≥ 10g/L. AST and ALT ≤ 2.5 \*the upper limit(UL) ,TBIL≤1.2\*the UL, CRE≤1.2\* the UL, and ALP≤5\* the UL). And the ECG should be normal * Good nutritional status,BMI:18\ 23Kg/ m2, PG-SGA ≤1,NRS 2002\<3score * No other previous neoplastic diseases, except for cured cervical carcinoma in situ skin basal carcinoma * No serious gastrointestinal diseases (moderate and severe duodenal and gastric ulcer, ulcerative colitis, Crohn's disease, etc.) * No AIDS and no diabetes * Clear mind, no communication barriers, able to answer questions * Voluntarily participate and sign the informed consent in person.

Exclusion criteria

* Patients with gastrointestinal dysfunction, intestinal obstruction, pyloric obstruction, Acute gastrointestinal bleeding * Patients who are allergic to nutritional therapy or have severe allergic constitution * Uncontrolled systemic diseases, such as severe liver disease (such as cirrhosis), kidney disease, respiratory diseases and so on. * Women who are pregnant or breastfeeding or no contraception and women with positive pregnancy test before receiving treatment * Special dietary requirements: such as no having a certain food or a vegetarian.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of acute radiation reactions12 monthsThis study mainly includes oral mucosa mucositis, salivary glands injury induced by radiotherapy, laryngoesophageal mucositis referring to The 2020 Expert Consensus on the Standardized Management of Radiation Oncology for nutrition-related radiation injury responses.

Secondary

MeasureTime frameDescription
Incidence of decline in nutritional status12 monthsanalysis by the clinical nutrition detection analyzer
Incidence of decline in quality of life scores(QOL)12 monthsIt is measured by a standard QOL table,including 12 questions.Each question is 5 points,so there are 60 points and 5 grades(51-60 points, 41-50 points, 31-40 points, 21-30 points,\<20 points).A higher score is a better life.
Self-rating Anxiety screening Scale(GAD-7)12 monthsA GAD-7 table would estimate one's anxiety according to the emotion of the past two weeks,including 9 questions and 27 points totally.There are 4 grades of anxiety, a LOWER score means a normal mind state. Actually,0-4 points is/are no anxiety.5-9 points represent slight anxiety .10-14 are in moderate anxiety.15-27 are severe anxiety,respectively.
Self-rating Scale for Depression Screening (PHQ-9)12 monthsA PHQ-9 table is a simplified Scale for Depression Screening,it would estimate one's depression emotion according to the mind of the past two weeks,including 9 questions and 27 points totally.There are 4 grades of depression, a LOWER score is equal to a GOOD mind.Actually,0-4 points is/are no depression.5-9 are depressed but not obvious.10-14 are in obvious depression.15-27 are severe depression,respectively.

Countries

China

Contacts

Primary ContactYunfei Xia, MD
xiayf@sysucc.org.cn13602805461

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026