Skip to main content
OpenTrials
Active, Not Recruiting

NCT Number: NCT07246850

A Randomized, Triple-blind, Placebo-controlled Study to Evaluate the Effects of a Throat Spray on the Incidence and Duration of Sickness

This is a randomized, triple-blind, placebo-controlled clinical trial evaluating the effects of Beekeeper's Naturals Propolis Immune Support Throat Spray on the incidence and duration of sickness over a 16-week period. The study will enroll 100 healthy adults aged 18 to 65.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Notify Me

Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Citruslabs

Las Vegas, Nevada, 89118, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Be male or female
  • Be aged 18-65
  • Meet at least one of the following criteria:

Work in a hospital or other healthcare setting Work in a school

  • Have a child/children under the age of 10
  • Be willing to take the test or placebo product once daily and complete study questionnaires every four weeks for the 16-week study period
  • Be willing to refrain from taking any over-the-counter products, herbal remedies, or supplements that target immune function during the study period and for two weeks prior.
  • Be willing to maintain their current diet, sleep schedule, and activity level for the duration of the study.
  • Be in good general health and not live with any uncontrolled chronic conditions.
  • Reside in the United States.

Exclusion criteria

  • Has undergone any surgeries or invasive treatments in the past six months or plans to undergo any during the study period
  • Anyone with seasonal allergies
  • Anyone who follows a restrictive diet (e.g., keto, vegan, raw, carnivore, etc.).
  • Anyone who got a vaccination in the last 2 weeks.
  • Anyone taking one or more prescription medications:

Corticosteroids: Prednisone (prednisone), Deltasone (prednisolone), Medrol (methylprednisolone), Decadron (dexamethasone), Cortef (hydrocortisone), Kenalog (triamcinolone), Flonase (fluticasone), Nasonex (mometasone) Biologics (Immunomodulating Agents): Humira (adalimumab), Enbrel (etanercept), Remicade (infliximab), Stelara (ustekinumab), Cosentyx (secukinumab), Taltz (ixekizumab), Orencia (abatacept), Simponi (golimumab), Xeljanz (tofacitinib), Rituxan (rituximab), Actemra (tocilizumab), Kineret (anakinra) DMARDs (Disease-Modifying Antirheumatic Drugs): Methotrexate (methotrexate), Plaquenil (hydroxychloroquine), Arava (leflunomide), Azulfidine (sulfasalazine), Imuran (azathioprine), CellCept (mycophenolate mofetil), Cytoxan (cyclophosphamide) JAK Inhibitors: Olumiant (baricitinib), Rinvoq (upadacitinib), Jakafi (ruxolitinib) Other Immunosuppressive Medications: Prograf (tacrolimus), Neoral, Sandimmune (cyclosporine), Rapamune (sirolimus), Zortress (everolimus)

  • Has had any major illness in the past three months.
  • Drinks heavily (defined as 8 or more alcoholic drinks per week for women or 15 or more alcoholic drinks per week for men).
  • Uses illicit drugs.
  • Has known allergies or hypersensitivities to any of the study product ingredients.
  • Is immunocompromised due to a medical condition or due to immunosuppressive medications or treatments.
  • Has any known autoimmune conditions.
  • Has any chronic health conditions that could impact participation in the study, including cancer, liver, or mental health disorders.
  • Has known serious allergic reactions requiring the use of an Epi-Pen.
  • Is currently pregnant, trying to conceive, or breastfeeding.
  • Is currently participating in another research study or plans to do so during the 16-week study period.
  • Has a history of substance abuse.
  • Is currently a smoker or has been a smoker in the past three months.

Treatment and study plan

Beekeeper's Propolis Throat Spray

Dietary Supplement

Participants will administer four sprays of Beekeeper's Propolis Throat Spray into the back of the mouth once daily in the morning for 16 weeks.

Placebo Throat Spray

Dietary Supplement

Participants will administer four sprays of a placebo throat spray into the back of the mouth once daily in the morning for 16 weeks.

Primary outcomes

  1. Changes in incidence and duration of sickness

    Time frame: Baseline, Weeks 4, 8, 12, and 16

    Self-reported via questionnaires comparing frequency and duration of illness episodes between groups

Secondary outcomes

  1. Perceived improvement in overall health

    Time frame: Baseline, Week 4, Week 8, Week 12, and Week 16

    Participants will report perceived changes in their overall health using self-administered questionnaires.

  2. Perceived improvement in overall well-being

    Time frame: Baseline, Week 4, Week 8, Week 12, and Week 16

    Participants will report their sense of overall well-being using self-administered questionnaires throughout the study.

  3. Perceived immune system support

    Time frame: Baseline, Week 4, Week 8, Week 12, and Week 16

    Participants will rate their perception of immune system support using self-administered questionnaires during the study.

Sponsors and collaborators

Lead sponsor

Beekeeper's Naturals Inc

Industry

Collaborators

  • Citruslabs

Registry information

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Nov 24, 2025
Registry last updated
Nov 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.