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Analysis of effects of Umbilical Cord Blood Transfusion in Bone Marrow Suppression caused by Treatment with Radiation Therapy with or without chemotherapy

Umbilical Cord Blood transfusion in Radiotherapy with or without Chemotherapy induced Bone Marrow Suppression- A Prospective Single institutional Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/089320
Enrollment
44
Registered
2025-06-23
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: D630- Anemia in neoplastic disease

Interventions

Intervention1: umbilical cord blood transfusion: umbilical cord blood transfusion in patients with radiotherapy with or without chemotherapy induced bone marrow suppression Control Intervention1: not

Sponsors

IPGMER and SSKM Hospital, Kolkata
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Performance status less than or equal to 2 More than 18 years of age. Persistent Grade 2 or higher hematological toxicities after chemotherapy or radiotherapy For at least 2 weeks. Toxicities will be assessed by EORTC CTCAE criteria and RTOG Radiation Toxicity Grading. Haemoglobin less than 10 gm/dl. / Total leucocyte count less than 3000/cumm. / Absolute neutrophil count less than 1500/cumm. / Platelet count less than 75000/cumm. Patients who will give consent to be included in the cord blood transfusion study.

Exclusion criteria

Exclusion criteria: Patients who have developed Hemotological toxicities due to causes other than radiation therapy and chemotherapy. Patients who have received growth factors, such as G-CSF, GM-CSF, erythropoietin, thrombopoetin within one weeks. Patients with distant metastasis.

Design outcomes

Primary

MeasureTime frame
If study shows that cord blood transfusion is quite effective in amelioration of anti-malignant therapy induced myelosuppression in Patients in our country, then this treatment can also be applied in anti-malignant therapy induced bone marrow suppression and also in other diseases causing bone marrow suppression.Timepoint: The complete blood count (CBC) of the patient will be assesed at baseline, 1 week and 2 weeks post transfusion

Secondary

MeasureTime frame
nilTimepoint: nil

Countries

India

Contacts

Public ContactDr Priyanka Das

IPGMER and SSKM Hospital Kolkata

alokeghoshdastidar@gmail.com9831118494

Outcome results

None listed

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