ClinicalTrials.Veeva

Menu

Effect of Nutritional Intervention Based on Prediction Model on Adult Umbilical Cord Blood Transplantation Patients

U

University of Science and Technology of China (USTC)

Status and phase

Not yet enrolling
Phase 2

Conditions

Nutrition Disorders

Treatments

Procedure: Individualized nutrition intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT06553274
Nutrition-2024

Details and patient eligibility

About

Based on the nutritional factor prediction model, the individualized nutritional management of patients with umbilical cord blood transplantation (UCBT) was carried out to observe the impact on the survival efficacy of patients.

Full description

The data of 80 UCBT patients were analyzed retrospectively, and the influence of nutritional parameters on the clinical outcome of UCBT patients was first confirmed, the skinfold thickness ≥20.5 mm and peripheral blood Alb < 33.6 g/L at 30 days after transplantation were the independent influencing factors of OS and DFS. In order to further verify the accuracy of the survival prediction model, the center intends to base on the model and aim at the nutritional parameters of patients 30 days after transplantation, a single-arm, single-center, phase II, prospective intervention trial was conducted to explore individualized nutrition management in UCBT patients.

Enrollment

67 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18-65 years old, conscious, with language communication skills;
  • UCBT patients to be performed;
  • Major organs without serious dysfunction;
  • The participants agreed to participate in the study and signed the informed consent form.

Exclusion criteria

  • Age < 18 years old or > 65 years old or with cognitive impairment can not complete this survey;
  • Failure or recurrence of transplantation;
  • Combined with severe other organ system diseases (such as severe cardiac insufficiency, autoimmune disease, active infection, severe trauma) ;
  • Patients who have difficulty collecting data to complete the nutritional intervention;
  • Patients who asked to withdraw from the study.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

67 participants in 1 patient group

Individualized nutrition intervention
Experimental group
Description:
Full-time clinical nutrition pharmacists evaluate the nutritional status of enrolled patients and design individualized nutrition management programs
Treatment:
Procedure: Individualized nutrition intervention

Trial contacts and locations

1

Loading...

Central trial contact

Xiaoyu Zhu, Ph.D; Lijuan Ning, M.D

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems