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Effects of compound Ma-ol-asal syrup on cancer-related fatigue

Phase 3
Recruiting
Conditions
eoplastic (malignant) related fatigue.
Neoplastic (malignant) related fatigue
R53.0
Registration Number
IRCT20191211045693N1
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
120
Inclusion Criteria

1.Age between 18- 70 years old
2. GI cancer (pathologically diagnosed)
3.Undergoing chemotherapy
4. Hemoglobin level at least 10g/dl
5. Hematocrit level at least 30% .
6. No clinical symptom of hypothyroidism
7. Visual Analogue Fatigue Scale (VAS)>=4

Exclusion Criteria

1. Heart disease with unstable conditions
2. Liver disease with unstable conditions
3. Disabling pulmonary disease
4. Positive history of hypersensitivity to honey and its compounds
5. Positive history of hypersensitivity to each component of the compound Ma-ol-asal syrup.
6. Uncontrolled pain.
7. An individual who uses treatment due to known psychiatric disease
8.Pregnancy.
9. Simultaneous use of drugs that affect fatigue.
10. kidney disease with unstable conditions
11. Severe infection
12. Serious accompanying disease.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Score of Fatigue Severity Visual Analogue Fatigue Scale. Timepoint: Week 0 (before the start of the intervention) and week 4 (after the start of the intervention). Method of measurement: Using Visual Analogue Fatigue Scale questionnaire.;Score of The Cancer Fatigue Scale. Timepoint: The weeks of 0 and 4 after treatment. Method of measurement: The Cancer Fatigue Scale questionnaire.
Secondary Outcome Measures
NameTimeMethod
Dyspepsia. Timepoint: Week 0 (before the start of the intervention) and week 4 (after the start of the intervention). Method of measurement: Likert scale.
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