ClinicalTrials.gg
CompletedNCT07538661Updated Apr 28, 2026

Metabolic Regeneration Registry for Periodontal Health (20-Patient Cohort).

An observational study in Chronic Periodontitis, Chronic Periodontitis Wth Diabetes Mellitus and Non-surgical Periodontal Treatment, sponsored by Amar h Zireg. Completed at 1 site in Algeria. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-04-28.

Sponsored by Amar h Zireg · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
20
Ages
18 Years and older
Sex
All
01

Study summary

This observational study documents the clinical outcomes of a proprietary, safe-to-swallow metabolic protocol for chronic gum disease. Based on 21 years of research and a focused 20-patient cohort, the study records visible clinical improvements in gingival inflammation and tissue color within 7 to 14 days. The protocol focuses on restoring the metabolic environment to achieve non-surgical periodontal pocket stabilization and natural tissue re-attachment.

02

Conditions studied

  • Chronic Periodontitis
  • Chronic Periodontitis Wth Diabetes Mellitus
  • Non-surgical Periodontal Treatment
  • Gingival Regeneration
  • Metabolic Repair

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Keywords

  • Gingival Regeneration
  • Metabolic Repair
  • Non-Surgical Periodontal Treatment
03

In context

Chronic Periodontitis

377 studies on the registry are indexed under Chronic Periodontitis; 21 are open to participants now.

This study's enrollment of 20 is below the median of 80 across 65 observational studies indexed under Chronic Periodontitis.

Browse Chronic Periodontitis studies →

Lead sponsor

Amar h Zireg is the lead sponsor of 3 studies on the registry; none are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients aged 18 to 75 years diagnosed with chronic periodontitis, characterized by gingival inflammation, bleeding on probing, and periodontal pocket depths of 4mm or greater. The population includes individuals seeking non-surgical alternatives for gum tissue recovery.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients (18-75) with documented chronic periodontitis and pocket depths >4mm.

Exclusion criteria

Exclusion Criteria:

  • Active oral or pregnancy
Terms in these criteria, in plain language(1)

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.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
20 participants (actual)
Target follow-up
30 Days
Patient registry
Yes

Interventions

  • Dietary supplementNutraceutical Bio-Active Oral Repair Formula (Food-Grade)

    Topical application of a proprietary, 100% food-grade (GRAS) nutraceutical formulation specifically designed for rapid gingival tissue regeneration and inflammation reversal. Key Performance Indicators: Speed: Clinical onset of action visible within 3 days. Safety: Completely safe for ingestion (edible), eliminating common side effects of chemical antiseptics like staining or taste alteration. Efficacy: Significant reduction in redness and bleeding (BOP) within 7 to 14 days, as demonstrated in our cohort of 20+ subjects. Mechanism: Supports the natural healing of the gum 'peau' (epithelium) through host-response modulation rather than harsh disinfection.

  • Dietary supplementNutraceutical Bio-Active Oral Repair Formula

    Topical application of a proprietary, 100% food-grade (GRAS) nutraceutical formulation specifically designed for rapid gingival tissue regeneration and inflammation reversal.Key Performance Indicators: Speed: Clinical onset of action visible within 3 days. Safety: Completely safe for ingestion (edible), eliminating common side effects of chemical antiseptics like staining or taste alteration. Efficacy: Significant reduction in redness and bleeding (BOP) within 7 to 14 days, as demonstrated in our cohort of 20+ subjects. Mechanism: Supports the natural healing of the gum 'peau' (epithelium) through host-response modulation rather than harsh disinfection."

06

What researchers measure

Primary outcomes

  1. Visible reduction in gingival inflammation and erythema (redness) observed within 7 to 14 days

    Time frame: 7 to 14 days

Secondary outcomes

  1. Measurement of periodontal pocket depth reduction and tissue stability at 6 weeks

    Time frame: 6 weeks

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Study locations

1 site
  • Zireg
    Bordj Bou Arreridj, Wilaya de Bordj Bou Arréridj 34000, Algeria
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Jan 2026 to primary completion in Feb 2026, 1 month.

Of 21 observational studies under Chronic Periodontitis, half reached primary completion within 9 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 17. This study's 1 month is below that.

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

Registered
Apr 13, 2026
First posted
Apr 20, 2026
StartActual
Jan 3, 2026
Primary completionActual
Feb 20, 2026
CompletionActual
Feb 26, 2026
Last update
Apr 28, 2026
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 Apr 28, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07538661
Lead sponsor
Amar h Zireg
Collaborators
Self funded
Responsible party
Amar h Zireg (sponsor investigator, Amar Zireg) — Sponsor-investigator
First posted
Apr 20, 2026
Start date
Jan 3, 2026
Primary completion
Feb 20, 2026
Completion
Feb 26, 2026
Last update
Apr 28, 2026

Oversight

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

Not currently enrolling

This study is completed, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

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