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Healthy effects of Royal Jelly in patients with colon cancer

Effect of Royal Jelly supplementation on anthropometric indices, fatigue, appetite, inflammatory indices and mortality in patients with colon cancer: a randomized controlled trial study

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110510006431N8
Enrollment
52
Registered
2024-07-11
Start date
2024-07-12
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Colon cancer. Malignant neoplasm of colon, unspecified

Interventions

Intervention 1: Intervention group: Patients in the intervention group will receive 2 royal jelly tablets daily, for 4 weeks while waiting for surgery. Manufacturer: Kooze Asal Company. Intervention 2

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age 18 to 65 years Diagnosed with colon cancer and needing surgery The cancer is in the second or third stage.

Exclusion criteria

Exclusion criteria: Pregnancy The immunodeficiency Progressive infection Disorder in the respiratory system (arterial oxygen pressure less than 70 mm Hg) Cardiovascular disorder Renal system disorder Hepatic disorders The level of hepatic enzymes is more than three times the upper limit of normal Serum hemoglobin level less than 8 g/dL with a sudden drop (more than 2 g/dL) in the last month. Total serum bilirubin greater than 2 mg/dL Serum creatinine greater than 2 mg/dL Creatinine clearance less than 60 ml/min

Design outcomes

Primary

MeasureTime frame
Fatigue. Timepoint: At the beginning of the research, after 4 weeks of intervention and before surgery. Method of measurement: The Fatigue will assess with analogue fatigue scale (VAFS) and fatigue severity scale (FSS).

Secondary

MeasureTime frame
Weight. Timepoint: At the beginning of the research, after 4 weeks of intervention and before surgery. Method of measurement: The weight is calculated by the scale.;Quality of life. Timepoint: At the beginning of the research, after 4 weeks of intervention and before surgery. Method of measurement: The quality of life will assess with questionnaire of cancer patients-Aronson (1987) and Fatigue with analogue fatigue scale (VAFS) and fatigue severity scale (FSS).;Body Mass Index (BMI ). Timepoint: At the beginning of the research, after 4 weeks of intervention and before surgery. Method of measurement: Body Mass Index ( BMI ) will calculate with BMI formula.;C-reactive protein. Timepoint: At the beginning of the research, after 4 weeks of intervention and before surgery. Method of measurement: 5 cc of blood is taken to measure the inflammatory factors and they are measured by ELISA kits.;Tumor necrosis factor-a. Timepoint: At the beginning of the research, after 4 weeks of intervention and before surgery. Method of measurement: 5 cc of blood is taken to measure the inflammatory factors and they are measured by ELISA kits.;Interleukin-6. Timepoint: At the beginning of the research, after 4 weeks of intervention and before surgery. Method of measurement: 5 cc of blood is taken to measure the inflammatory factors and they are measured by ELISA kits.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahdi Shadnoush

National Nutrition and Food Technology Research Institute

shadnoush@sbmu.ac.ir+98 21 2240 1423

Outcome results

None listed

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