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A study to assess the effect of Resveratrol and Copper in reducing toxicity during bone marrow transplantation for multiple myeloma.

Not Applicable
Conditions
Health Condition 1: null- Patients undergoing autologous hematopoietic stem cell transplantation for multiple myeloma at Tata Memorial Centre.
Registration Number
CTRI/2018/02/011905
Lead Sponsor
TMC Research Administrative Council
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Male or female patients 18 years and above.

2.Patients who have given written informed consent

3.Patients with performance status of 0,1 or 2 (ECOG scale)

4.Patients of multiple myeloma receiving melphalan- 200 mg/m2 (MEL-200 mg/m2)

5.Patients who have creatinine clearance > 50 ml/min

6.Patients with serum bilirubin levels < 2mg/dl and serum liver enzymes (ALT or AST or both) less than 5 times the upper limit of normal value.

Exclusion Criteria

1.Patients who are on NSAIDs , aspirin ,antioxidants or systemic steroids for more than 3 months and the last dose taken within the last one week.

2.Patients being treated for active infection at the time of starting high dose chemotherapy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To determine the plasma and saliva levels of inflammatory cytokines (PGE2, TNF-α, INF-gamma, IL-6, IL-1 and CRP) at pre-defined time-points following administration of 4-dose-levels of R-Cu in patients receiving autologous transplant for multiple myeloma.Timepoint: To determine the plasma and saliva levels of inflammatory cytokines (PGE2, TNF-α, INF-gamma, IL-6, IL-1 and CRP) 2 days prior to start of high dose chemotherapy, on day 0 (ie day of stem cell infusion) and then every 3rd day till day 21 post transplant.
Secondary Outcome Measures
NameTimeMethod
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