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Effect of royal jelly in treatment of stroke

The effects of royal jelly supplementation on inflammatory status, oxidative stress, mental health, cognitive function, disease severity and quality of life in patients with ischemic stroke

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180818040827N4
Enrollment
64
Registered
2021-10-16
Start date
2021-11-22
Completion date
Unknown
Last updated
2022-08-29

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

Conditions

Ischemic stroke. Cerebellar stroke syndrome

Interventions

Intervention 1: Intervention group: The intervention group will receive one tablet of Royal Jelly (containing 1000 mg of Royal Jelly powder) daily after breakfast for 12 weeks. Royal Jelly supplement

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 80 Years

Inclusion criteria

Inclusion criteria: Confirmed diagnosis of ischemic stroke by a neurologist NIHSS score of 5-20 An absence of previous stroke or or MRS score of = 1 for those with previous stroke Ischemic stroke of non-brain stem area age of 45-80 Not following specific dietary regimen in previous 3 months Not taking multivitamins and antioxidant supplements in the previous 3 months Non pregnant and lactating women No other diseases such as acute kidney, liver, heart, other neurological diseases, malignancies, no asthma, allergies and dermatitis Not suffering from mental retardation (mental disabilities) Not taking drugs that interfere with Royal Jelly supplementation (warfarin) Lack of sensitivity and allergy to honey and its products

Exclusion criteria

Exclusion criteria: Unwillingness to continue the study for any reason Adherence of less than 80% to the intervention (taking less than 80% of Royal Jelly supplement that should be taken during the 12 weeks of the intervention will be considered low adherence) Recurrence of stroke Death Use of antioxidant and multivitamin supplements during the study Prescription of warfarin during the study Gastrointestinal side effects or allergies caused by taking Royal Jelly supplement Diagnosis of other diseases such as kidney, autoimmune and malignancies during the study

Design outcomes

Primary

MeasureTime frame
Superoxide dismutase. Timepoint: At baseline and after 12 weeks. Method of measurement: Colorimetric method.;Glutathione peroxidase. Timepoint: At baseline and after 12 weeks. Method of measurement: Colorimetric method.;Malonaldehyde. Timepoint: At baseline and after 12 weeks. Method of measurement: Colorimetric method.;Total antioxidant capacity. Timepoint: At baseline and after 12 weeks. Method of measurement: Colorimetric method.;Total oxidant status. Timepoint: At baseline and after 12 weeks. Method of measurement: Colorimetric method.;Nitric oxide. Timepoint: At baseline and after 12 weeks. Method of measurement: Colorimetric method.;Brain derived neurotrophic factor. Timepoint: At baseline and after 12 weeks. Method of measurement: ELISA method.;Modified Rankin Scale. Timepoint: At baseline and after 12 weeks. Method of measurement: Questionnaire.;Stroke specific quality of life. Timepoint: At baseline and after 12 weeks. Method of measurement: Questionnaire.;Cognitive function. Timepoint: At baseline and after 12 weeks. Method of measurement: MMSE questionnaire.;Fatigue score. Timepoint: At baseline and after 12 weeks. Method of measurement: FSS questionnaire.;Uric acid. Timepoint: At baseline and after 12 weeks. Method of measurement: Colorimetry.;C-reactive protein. Timepoint: At baseline and after 12 weeks. Method of measurement: Colorimetry.;Erythrocyte sedimentation rate. Timepoint: At baseline and after 12 weeks. Method of measurement: Colorimetry.;Blood pressure. Timepoint: At baseline and after 12 weeks. Method of measurement: sphygmomanometer.;Lipid profile. Timepoint: At baseline and after 12 weeks. Method of measurement: Colorimetry.;Fasting Blood Glucose. Timepoint: At baseline and after 12 weeks. Method of measurement: Colorimetry.

Secondary

MeasureTime frame
Stress score. Timepoint: At baseline and after 12 weeks. Method of measurement: DASS-21 questionnaire.;Depression score. Timepoint: At baseline and after 12 weeks. Method of measurement: DASS-21 questionnaire.;Anxiety score. Timepoint: At baseline and after 12 weeks. Method of measurement: DASS-21 questionnaire.;Appetite score. Timepoint: At baseline and after 12 weeks. Method of measurement: SNAQ questionnaire.;Mid arm circumference. Timepoint: At baseline and after 12 weeks. Method of measurement: Tape meter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Amnai

Esfahan University of Medical Sciences

rezaamani@hotmail.com+98 31 3668 1378

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Aug 24, 2026