Health Condition 1: Z768- Persons encountering health services in other specified circumstances
Conditions
Interventions
Intervention1: NUVASTATIC® (C5OSEW5050ESA): Tablet 1000 mg TDS,Oral for six weeks
Control Intervention1: Placebo: Tablet TDS,Oral for six weeks
Sponsors
Natureceuticals Sdn Bhd
NOTROXRESEARCH PVT LTD
Eligibility
Inclusion criteria
Inclusion criteria: 1. Males or females, >= age 18 2. Patients with solid tumors, Stage I-IV 3. Patients who received, receiving or plan to receive of chemotherapy and/or >= 1 week of radiotherapy. 4. ECOG 0-2 5. Life expectancy >= 6 months 6. Ability and willingness to provide written informed consent and comply with study requirement Inclusion criteria for randomization: 1. At enrollment, subject should have received >= 2 cycles (21-day or 28 â??day cycle) of chemotherapy or >= 1 week of radiotherapy 2. Worsening of fatigue scoring as assessed by BFI questionnaire compared to previous scoring, defined as mild to moderate, moderate to severe, mild to severe, or newly developed fatigue
Exclusion criteria
Exclusion criteria: 1. Known allergy to CANSSUFIVE® Nuvastatic (C5OSEW5050ESA) or any of the excipient used in the preparation of the investigational product 2. Any other known existing condition that contraindicate with the use of investigational product 3. Inability to take or consume the investigational product per protocol specified route of administration including peptic ulcer disease, chronic gastritis, hypotension and systolic blood pressure 4. Inability to understand local language (s) for which BFI, EORTC-QLQ- C30, FACIT-F, visual analogue scale for fatigue questionnaire 5. Any condition (e.g. Psychological, geographical etc.) that does not permit compliance with study or follow up procedures 6. Participation in any other clinical study using investigational medicinal product or device within 28 days prior baseline visit 7. Treatment with medications or supplements frequently associated with fatigue, such as interferon (within the last four months), beta-blockers, calcium channel blockers, benzodiazepines, sedating antihistamines, antidepressants, antipsychotics, or melatonin. In select instances, patients using these medications may be enrolled if, in the opinion of the investigators, their fatigue is clearly unrelated to the medication. 8. Untreated or uncontrolled comorbidities that influence fatigue, including thyroid disorders (TSH > 5 mcIU/mL), anemia (Hemoglobin 9. Chronic renal failure patients with raised serum potassium levels and abnormal renal function 10. Untreated sleep disorders such as obstructive sleep apnea or restless leg syndrome 11. Decompensated cirrhosis (encephalopathy, gastrointestinal bleeding, ascites, bilirubin > 2) within the last six months 12. Patients planning to travel outside the time zone during the study period 13. Known or suspected significant gastrointestinal motility disorder, obstruction, or structuring disease 14. Severe malnutrition according to WHO criteria. 15. Upon examination, patient may deemed to have any of the following conditions: a. Bipedal oedema b. Visible severe wasting c. Weight for height more than 3 standard deviations below the median of international reference population d. Fever related to systemic infection (especially Gram-negative coliforms such as Escherichia coli and Klebsiellapneumoniae), neutropenic sepsis e. Respiratory distress f. Heart failure g. Electrolyte abnormalities (hypophosphataemia, hypokalemia/ hyperkaliemia, hypoglycemia etc.) h. Marked anorexia i. Profuse diarrhea j. Shock 16. The patient is female and : a. is pregnant or fertile and is not practicing adequate methods of contraception, b. is planning to become pregnant within 1 month of the study, c. is breastfeeding. Note: Females who are breastfeeding should not be discouraged from breastfeeding for the sole purpose of enrolling in the study. Females who choose to defer breastfeeding until 5 days after the last dose of study drug to allow elimination of drug from breast milk will be eligible.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate efficacy of CANSSUFIVE® Nuvastatic (C5OSEW5050ESA) in Improving Fatigue in Patients with Solid Stage I - IV Tumors.Timepoint: Day -21 to Day 63 | — |
Secondary
| Measure | Time frame |
|---|---|
| o evaluate the safety and tolerability of CANSSUFIVE® Nuvastatic (C5OSEW5050ESA) in Patients with Solid Stage I - IV Tumors.Timepoint: Day -21 to Day 63 | — |
Countries
India
Contacts
Public ContactMeena Dalal
IR Innovate Research Private Limited
Outcome results
None listed