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Inflammatory Cytokine ExpressionNCT07367451

Effects of Propolis Flavonoids on TLR4 Signaling and Inflammation in Human PDLSCs In Vitro

An observational study of Inflammatory Cytokine Expression, run by Cairo University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Official record
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Trial summary

This in-vitro study evaluated the effects of a flavonoid-rich propolis extract on Toll-like receptor 4 (TLR4) signaling and inflammatory cytokine expression in human periodontal ligament stem cells (PDLSCs). Read more about this study

Who is it for?
Any age
Conditions the study is for
Inflammatory Cytokine Expression
What is being tested?
Flavonoid extract from propolis and no medication added
How many people
20 participants
Where
No sites listed yet
Study dates
25 Jan 2026to 10 Feb 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: in vitro study

Who may be able to join

  • invitro study on Human Periodontal Ligament Stem Cells

Who cannot join

  • none

About this study

Official title: Effect of Propolis-Derived Flavonoid Extract on TLR4 Signaling and Inflammatory Cytokine Expression in Human Periodontal Ligament Stem Cells (PDLSCs): An In-Vitro Study

This in-vitro study evaluated the effects of a flavonoid-rich propolis extract on Toll-like receptor 4 (TLR4) signaling and inflammatory cytokine expression in human periodontal ligament stem cells (PDLSCs). PDLSCs were treated with propolis flavonoids under baseline conditions and following lipopolysaccharide (LPS)-induced inflammation, with untreated cells serving as controls. TLR4 gene expression was analyzed using PCR, while levels of pro-inflammatory cytokines (IL-1β, IL-6, and TNF-α) were quantified by ELISA. Cell viability and cytotoxicity at different extract concentrations were assessed using the MTT assay. The study aimed to determine the immunomodulatory and cytocompatible potential of propolis flavonoids in regulating inflammatory responses in PDLSCs.

Being tested
Flavonoid extract from propolis, no medication added
Keywords
TLR4, flavonoid-rich propolis, Periodontal ligament, stem cells

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Flavonoid extract from propolisDrug

    Preparation of Propolis Flavonoid Extract

    Concentrations for testing:

    5 µg/mL 10 µg/mL 20 µg/mL

  • no medication addedOther

    No medication will be added to the second group

Study groups in NCT07367451
Study groupRoleWhat they receive
Isolated PDLSCs, and adding Flavonoid extract from propolisNot described
Receives: Drug: Flavonoid extract from propolis
Isolated PDLSCs, no material addedNot described
Receives: Other: no medication added

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. TLR4 expression

    To evaluate the expression of TLR4 in PDLSCs after treatment with propolis flavonoid extract.

    Measured: 48 hours

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Jan 2026
  2. Study start25 Jan 2026 (estimated)
  3. Primary completion30 Jan 2026 (estimated)
  4. Study completion10 Feb 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
20 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07367451
Sponsor's protocol ID
12/2025
Status last verified
Jan 2026
First submitted
18 Jan 2026
Last updated
5 Feb 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Inflammatory Cytokine Expression, run by Cairo University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 5 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

TLR4 expression (time frame: 48 hours). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Feb 2026.

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