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Efficacy of thalidomide in the treatment of patients with non-transfusion dependent thalidomide anemia

Efficacy of thalidomide in the treatment of patients with non-transfusion dependent thalidomide anemia

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000033205
Enrollment
Unknown
Registered
2020-05-24
Start date
2020-05-10
Completion date
Unknown
Last updated
2020-05-25

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

Conditions

Thalassemia

Interventions

Case series:The first stage: thalidomide 25mg / day oral, treatment 3 months (12 weeks)
the second stage: first stage: thalidomide reduction of 12.5mg / day oral, treatment 3 months (12 weeks ).

Sponsors

The People's Liberation Army Joint Logistics Support Unit 923th Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients with clinical and genetic diagnosis are NTDT patients; 2. Aged between 18 and 65 years old, male or female; ECOG physical strength score is 0 to 2 points; 3. Those who have received thalidomide (50mg / day) and are effective (hemoglobin rises more than 1g / dL); 4. Sign the written informed consent before the test.

Exclusion criteria

Exclusion criteria: 1. A history of blood transfusion or the use of hydroxyurea, Yisuishengxue granules and other red blood cell-increasing drugs within 3 months before the inclusion; 2. Women in pregnancy and lactation and subjects of childbearing age who do not want to take contraceptive measures; 3. Those with severe cardiopulmonary disease and abnormal liver function; with severe primary diseases such as cerebrovascular, cardiovascular, liver, kidney, and tumor; with anemia caused by other reasons, such as autoimmune hemolytic anemia; 4. Those who are allergic to the ingredients of this medicine; 5. Psychotic patients; 6. Those who participated in clinical trials of other drugs within the past month; 7. Those with a history of venous or arterial thrombosis; 8. The investigator decides that it is not suitable to participate in this research.

Design outcomes

Primary

MeasureTime frame
Hemoglobin;Hemolysis index;Safety assessment;

Countries

China

Contacts

Public ContactXiao-Lin Yin

The People's Liberation Army Joint Logistics Support Unit 923th Hospital

yin-xl@163.com+86 13321717899

Outcome results

None listed

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