CClinicalTrials.gg
Status unknownNCT04672850Updated Apr 12, 2022

The Effect of Probiotic and Zinc Supplementation on the Common Cold

An interventional study of Probiotic and Placebo in Common Cold, sponsored by Lund University. Status unknown at 1 site in Sweden. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-04-12.

Sponsored by Lund University · Not applicable, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Apr 2022), so the status shown — last known as Enrolling by invitation — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

The purpose with this study is to investigate the preventative effect of a supplement containing a combination of probiotic bacteria and fungi as well as zinc on the common cold. The hypothesis is that it will shorten the duration, alleviate the severity of symptoms or even decrease the number of infectons during the intervention period. This study is a randomzed placebo controlled human study were healthy adults will consume the supplement for three months.

02

Conditions studied

  • Common Cold

Browse trials for

03

In context

Common Cold

180 studies on the registry are indexed under Common Cold; 22 are open to participants now.

This study's planned enrollment of 100 is below the median of 167 across 151 interventional studies indexed under Common Cold.

Browse Common Cold studies →

Lead sponsor

Lund University is the lead sponsor of 230 studies on the registry; 37 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Healthy adults

Exclusion criteria

Exclusion Criteria:

  • Diagnosed gastrointestinal disorders
  • Autoimmune diseases or immuno compromized
  • Antibiotic treatment in the last month
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
100 participants (estimated)

Study arms

  • Placebo comparator
    Placebo

    Rice flour

    Dietary Supplement: Placebo

  • Active comparator
    Probiotic

    Probiotic bacteria, yeast, zinc and rice brand

    Dietary Supplement: Probiotic

Interventions

  • Dietary supplementProbiotic

    The participants will consume 2 capsules daily for three months

  • Dietary supplementPlacebo

    The participants will consume 2 capsules daily for three months

06

What researchers measure

Primary outcomes

  1. Symptoms severity

    Decrease in the severity of symptoms will be determined using a common cold questionnaire.

    Time frame: Three months

Secondary outcomes

  1. Composition of gut and oral microbiome

    Change in gut and oral microbiome will be measured using 16SrRNA and 18SrRNA sequencing

    Time frame: Three months

  2. IgA

    Changes in levels of IgA in saliva and/or feces will be measured using ELISA

    Time frame: Three months

  3. Duration of symptoms

    Decrease in duration of cold will be determined using a common cold questionnaire

    Time frame: Three months

  4. Number of colds

    Decrease in number of colds will be determined using a common cold questionnaire

    Time frame: Three months

07

Study locations

1 site
  • Lunds universitet
    Lund, Sweden
08

References and documents

Individual participant data

Plan to share: No — Only group data will be shared

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 12, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04672850
Lead sponsor
Lund University
Collaborators
Coradil AB
Responsible party
Åsa Håkansson (Assoc. Prof., Lund University) — Principal investigator
First posted
Dec 17, 2020
Start date
Jan 27, 2021
Primary completion
Nov 2022 (estimated)
Completion
Nov 2022 (estimated)
Last update
Apr 12, 2022

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2022. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion