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Treatment of thalassemia intermedia with decitabin combined with hydroxycarbamide

Treatment of thalassemia intermedia with decitabin combined with hydroxycarbamide

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-13004111
Enrollment
Unknown
Registered
2013-05-03
Start date
2013-11-25
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

thalassemia intermedia

Interventions

one cohort:combining decitabine and hydroxycarbamide

Sponsors

303rd Hospital of the People`s Liberation Army of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. patients should be diagnosed as thalassemia intermedia by genotype and clinic manifestion; 2. patients should be aged between 16 and 50 yrs old, with ECOG between 0 and 2; 3. Informed consent should be signed before the start of clinic trail.

Exclusion criteria

Exclusion criteria: 1.Any treatment such as blood transfusion, hydroxycarbamide, or yisuishengxue granules in 2 months before including; 2. Pregnancy, breast feeding, or patients in reproductive ages without any measurements of contraception; 3. Patients accompany sever pulmonary or cardiac diseases, liver function abnormal, or sever primary disease of liver, kidney, tumor, and so on; 4. Patients who are allergy to decitabien or hydroxycarbamide; 5. Patients of mental disease; 6. Patients take part in orther kinds of clincic trails in one month; 7. Other conditions that investigaters considered to be not suitable for this clinic trail.

Design outcomes

Primary

MeasureTime frame
hemoglobi;

Secondary

MeasureTime frame
hemoglobine F;

Countries

China

Contacts

Public ContactXiao-lin Yin

303rd Hospital of PLA

yin-xl@163.com+86 0771 2870496

Outcome results

None listed

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