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Health related quality of life after single unit umbilical cord blood transplantation versus HLA-matched related allogeneic hematopoietic stem cell transplantation for patients aged = 14 years

Health related quality of life after single unit umbilical cord blood transplantation versus HLA-matched related allogeneic hematopoietic stem cell transplantation for patients aged = 14 years

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800014653
Enrollment
Unknown
Registered
2018-01-26
Start date
2018-02-15
Completion date
Unknown
Last updated
2018-02-26

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

Conditions

blood disease after single unit umbilical cord blood transplantation or HLA-matched related allogeneic hematopoietic stem cell transplantation

Interventions

group treated with UCBT:Patients are treated with single unit umbilical cord blood transplantation
group treated with HLA-matched related HSCT:Patients are treated with HLA-matched related hematopoetic stem cell transplantation

Sponsors

Anhui Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with hemaotogical diseases needed allo-HSCT according to Expert consensus on the treatment of hematological diseases by allogeneic hematopoietic stem cell transplantation in China; 2. Patients aged = 14 years, any gender, any race; 3. No severe organ failure and active infection; 4. Patients and their families voluntarily carry out UCBT or HLA-matched related HSCT and sign informed consent; 5. Patients and their families voluntarily participate in this research and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Serious viscera dysfunction or disease, such as serious diseases and function disorder in heart, liver, kidney and pancreas; 2. Patients aged less than 14 years; 3. Patients with drug dependence, uncontrolled mental disease or cognitive impairment; 4. Participate in other similar clinical researches in 3 months; 5. Researchers think that the patient doesn't fit into the group (e.g., patients are expected to be discontinue because of funding problems).

Design outcomes

Primary

MeasureTime frame
180d FACT-BMT total score;

Secondary

MeasureTime frame
FACT-BMT Physical Well-Being (PWB) Score;FACT-BMT Social/Family Well-Being (SWB) Score;FACT-BMT Emotional Well-Being (EWB) Score;FACT-BMT Functional Well-Being (FWB) Score;FACT-BMT Trial Outcome Index (TOI);FACT-G total score;SF-36 Physical Functionin (PF) score;SF-36 Role-Physical (RP) score;SF-36 Bodily Pain (BP) score;SF-36 General Health (GH) score;SF-36 Vitality (VT) score;SF-36 Social Functioning (SF) score;SF-36 Role-Emotional (RE) score;SF-36 Mental Health (MH) score;Cumulative incidence of acute GVHD;Cumulative incidence of chronic GVHD;180d transplant related mortality (TRM);relapse rate;Cumulative rate of neutrophil engraftment;Cumulative rate of platelet engraftment;neutrophil engraftment time;platelet engraftment time;

Countries

China

Contacts

Public ContactZimin Sun

Department of Hematology, Anhui Provincial Hospital

zmsun_vip@163.com+86 13605518126

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026