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Nutritional Status of Patients After Hematopoietic Stem Cell Transplantation

A Survey of Nutritional Status of Patients After Hematopoietic Stem Cell Transplantation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04146870
Enrollment
200
Registered
2019-10-31
Start date
2018-10-01
Completion date
2026-12-30
Last updated
2026-03-19

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

Conditions

Hematopoietic Stem Cell Transplantation, Nutrition

Brief summary

The main objectives of this study were :(1) to comprehensively and systematically evaluate the nutritional status of patients after hematopoietic stem cell transplantation. (2) to explore the effect of nutritional factors on the prognosis of patients treated by hematopoietic stem cell transplantation.

Detailed description

This study is devised to investigate nutritional status in patients who have undergone hematopoietic stem cell transplantation in the First Affiliated Hospital of Soochow University. Evaluation time points include the day before receiving conditioning regimen, post-transplantation 180 days, the nutritional status of patients were systematically evaluated from the aspects of food intake, physical activity level, body composition, blood biochemistry, etc. Also, the effect of nutritional factors on prognosis of hematopoietic stem cell transplantaion patients will be evaluated.

Interventions

not have

Sponsors

The First Affiliated Hospital of Soochow University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients who undergo hematopoietic stem cell transplantation in the First Affiliated Hospital of Soochow University. * Having a life expectancy of more than 3 months

Exclusion criteria

* Not willing to participate in the investigation * Age less than 15 years old or more than 80 years old

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline fat free mass at 6 months6 monthsBody composition analyzer INBO DY S10 (bioelectrical impedance method) is used to analyze the content of fat free mass( kilograms)
Change from Baseline fat mass at 6 months6 monthsBody composition analyzer INBODY S10 (bioelectrical impedance method) is used to analyze the content of fat mass( kilograms)
Change from Baseline food intake at 6 months6 months24-hour dietary record and semi-quantitative food frequency questionnaire are used to evaluate the eating condition of patients
Change from Baseline albumin level in blood at 6 months6 monthsThe content of albumin in blood is determined.

Secondary

MeasureTime frameDescription
Overall survial3 yearsIt is measured from the date of entry into this trial to the date of death from any cause; patients not known to have died at last follow-up are censored on the date they were last known to be alive
Event free survival3 yearsIt is measured from the date of entry into this trial to the date of relapse from CR, or CRi, or death from any cause; patients not known to have any of these events are censored on the date they were last examined.

Countries

China

Contacts

CONTACTSheng-Li Xue, M.D.
slxue@suda.edu.cn+86 512 67781139

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 20, 2026