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Investigating the effect of Megestrol Acetate and Omega-3, L-Carnitine, and L-Arginine on improving the appetite status of patients with advanced cancer.

Investigating the effect of Megestrol Acetate and Omega-3 and Megestrol Acetate, L-Carnitine, and L-Arginine on improving the appetite status of patients with advanced cancer.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250205064658N2
Enrollment
63
Registered
2025-03-08
Start date
2025-03-10
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Advanced cancer disease. Malignant neoplasms

Interventions

Sponsors

Khoram-Abad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 70 Years

Inclusion criteria

Inclusion criteria: Advanced cancer diagnosis by an oncologist (based on the TMN score and type of cancer) Anorexia having a minimum score of 3 in the symptoms section (provided that the score of 3 pertains to anorexia or lack of appetite) Minimum score of 1 in the dietary intake section Minimum score of 0 in the recent current weight section Minimum score of 0 in the activity section (with a minimum total score of 4) in the PG-SGA questionnaire Patients aged 45-70 years with weight loss due to advanced cancer (weight loss of at least 2.5 kg over 6-8 weeks or weight loss of at least 5% over the last 6-12 months) Not using other appetite-stimulating and weight-gaining supplements during the study No history of allergy to L-Arginine, L-Carnitine, Omega-3, and Megestrol Acetate Willingness to participate in the study.

Exclusion criteria

Exclusion criteria: Patients' refusal during the study. Occurrence of side effects Development of acute liver and kidney diseases Development of coagulation disorders Non-use of L-Arginine, L-Carnitine, Omega-3, and Megestrol Acetate during the study.

Design outcomes

Primary

MeasureTime frame
Reduction in the PG-SGA questionnaire score. Timepoint: At the beginning of the study (before the intervention started), 21 days and 31 days after the intervention began. Method of measurement: PG-SGA questionnaire.;Weight gain. Timepoint: At the beginning of the study (before the intervention started), 21 days and 31 days after the intervention began. Method of measurement: scale (for measuring weight changes).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Kharazmkia

Khoram-Abad University of Medical Sciences

kharazmkia@gmail.com+98 66 3330 0661

Outcome results

None listed

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