ClinicalTrials.gg
Enrolling by invitationNCT06810752Updated Feb 6, 2025

Thyme Honey for Management of Oral Lichen Planus

A Phase 1/2 interventional study of thyme honey and Triamcinolone Acetonide in Oral Lichen Planus, sponsored by British University In Egypt. Enrolling by invitation at 1 site in Egypt. Per ClinicalTrials.gov, last updated 2025-02-06.

Sponsored by British University In Egypt · Phase 1/2, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Feb 2025, 1 year 9 months ago, but the record still lists the study as enrolling by invitation.
  • Registered 3 months after the study started (first participant enrolled Oct 2024, registered Jan 2025).
Phase
Phase 1/2
Study type
Interventional
Enrollment
30
Allocation
Randomized
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 35 studies in Lichen Planus, Oral with a site in Egypt — 5 open to participants now, 7 under way, 2 of them phase 3. Lichen Planus, Oral · Egypt.

Planned enrollment
16th of 23
30 · median 39
Started
2024
with 3 others
Phase 1/2
Only one
of the 35
Registered
28th of 35
by date
Lead sponsor
2 of 35
British University In Egypt

Among the 35 studies in Lichen Planus, Oral with a site in Egypt, this one is the 16th largest by planned enrollment of the 23 interventional ones that give a count, is one of 4 that started in 2024, is the only one in phase 1/2, and was the 28th registered.

Lichen Planus, Oral

142 studies on the registry are indexed under Lichen Planus, Oral; 27 are open to participants now.

Browse Lichen Planus, Oral studies →

Open to participants now

5 of the 35 studies in Lichen Planus, Oral with a site in Egypt are open now. Recruiting first, the newest first:

All 5 open studies →

A study can be open while its sites in Egypt have not opened yet or have stopped. Only those recruiting at a site in Egypt →

Who these studies take

Of the 14 Lichen Planus, Oral studies recruiting now, 10 (71%) set no upper age limit and 2 (14%) stop at 75 or younger; 3 take children under 18; 3 take healthy volunteers.

This study: all sexes · no healthy volunteers.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 35 studies in Lichen Planus, Oral with a site in Egypt, or all of them as a file.
02

Study summary

the study aimed to assess the effect of topical application of thyme honey in comparison to 0.1% triamcinolone acetonide oral paste on the relief of pain and clinical improvement in patients with OLP

03

Conditions studied

  • Oral Lichen Planus

Browse trials for

Keywords

  • Oral Lichen Planus
  • Thyme Honey
  • triamcinolone acteonide
04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:• Patients clinically and histopathologically (if required) diagnosed as suffering from OLP.

  • Patients free from any visible oral lesions other than OLP.
  • Patients who agreed to take supplied medications.
  • Patients who agreed for the (when required).

Exclusion Criteria:• •Patients suffering from any systemic disease.

  • Treatment with any systemic treatment such as systemic , other drugs or non-steroidal anti-inflammatory drugs at least eight weeks.
  • Treatment with any oral topical medications for at least four weeks prior to the study.
  • Pregnant and lactating women.
  • In addition, no consideration was given to patients with a history of to honey.
Terms in these criteria, in plain language(4)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Biopsy and archival tissue

A biopsy takes a small piece of tissue to examine. “Archival tissue” is a sample already taken, for example at diagnosis, and kept by the hospital.

Whether a stored sample will do depends on when it was taken, how much there is and what the study needs. Ask whether the study accepts your stored sample or needs a new biopsy.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
30 participants (estimated)

Study arms

  • Active comparator
    Thyme Honey group

    Topical application of Thyme Honey

    Dietary Supplement: thyme honey

  • Placebo comparator
    Control group

    Topical application of Triamcinolone acetonide

    Drug: Triamcinolone Acetonide

Interventions

  • Dietary supplementthyme honey

    Topical application on the oral mucosa

  • DrugTriamcinolone Acetonide

    Topical application on the oral mucosa

06

What researchers measure

Primary outcomes

  1. VAS score assessement

    Pain intensity

    Time frame: 1 month

Secondary outcomes

  1. measurement of salivary level of miRna155

    Time frame: 1 month

07

Study locations

1 site
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Oct 2024 (actual). Primary completion is estimated for Feb 2025, 4 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 23, 2025
First posted
Feb 6, 2025
StartActual
Oct 12, 2024
Primary completionEst.
Feb 2025
CompletionEst.
Mar 2025
Last update
Feb 6, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 6, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06810752
Lead sponsor
British University In Egypt
Responsible party
Sponsor
First posted
Feb 6, 2025
Start date
Oct 12, 2024
Primary completion
Feb 2025 (estimated)
Completion
Mar 2025 (estimated)
Last update
Feb 6, 2025

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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