Haematological Abnormality Clinical Trial
Official title:
A Prospective Phase II Randomized, Blinded Study to Demonstrate the Effectiveness of Jobelyn for the Treatment of Breast Cancer Patients.
To determine the effective functionality/potency of Jobelyn as an immunologic and haematologic booster in Breast cancer patients (start-off), thus improving the outlook and the quality of life of such patients generally
Status | Recruiting |
Enrollment | 60 |
Est. completion date | January 2018 |
Est. primary completion date | October 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: Women with histologically confirmed breast cancer who had undergone complete or segmental mastectomy plus axillary node dissection were included Exclusion Criteria: Patients were excluded if they had distant metastases residual disease in the breast or axilla other serious medical illnesses, or a previous cancer. Women considering pregnancy or using hormones were excluded Patients who refuse to sign consent form |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Nigeria | Lagos State University | Ikeja | Lagos |
Nigeria | Lagos State University Teaching Hospital | Ikeja | Lagos |
Lead Sponsor | Collaborator |
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Lagos State University |
Nigeria,
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* Note: There are 14 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Natural Killer Cells Expression | Evaluation of the expression of activated natural killer cells CD3-CD56+CD69+ after treatment with Jobelyn | 6 months | No |
Secondary | Use of health related quality of life measures tool Safety Fractor-36 and self reporting questionnaires | Subjects would use form Safety Fractor-36 to score aspects of well-being | 6 months | No |
Secondary | Hematocrit Changes | Changes in levels of hematocrit after treatment with Jobelyn | 6 months | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03137745 -
Coagulation Profile of Patients Undergoing CRS(Cytoreductive Surgery) and Hyperthermic Intraperitoneal Chemotherapy
|
N/A |