The Efficacy of Salvia Officinalis Gel in the Treatment of Periodontitis CLINICAL TRIAL

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age25-75
SponsorUniversity of Baghdad

About this trial

From each participant, two sites of periodontal pockets ( ≥ 5 mm ) were selected and randomly allocated to either the test site (treated with scaling and RSD with S. officinalis gel) or the control site (treated with scaling and RSD alone).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

patients diagnosed with periodontitis had at least 20 natural teeth, with probing pocket depth (PPD) ≥ 5 mm and attachment loss ≥ 4 mm

Disqualifiers

Exclusion criteria were pregnancy, lactation, smoking, and any systemic disease that might affect periodontal disease progression or require antibiotic usage. Likewise, patients who had received anti-inflammatory medications or antibiotics in the preceding three months were excluded.

Trial design

Design model

Single group

Treatments tested in this trial

  • Salvia officinalis Gel

    Dietary supplement

    From each participant, two sites of periodontal pockets ( ≥ 5 mm ) were selected and randomly allocated to either the test site (treated with scaling and RSD with S. officinalis gel) or the control site (treated with scaling and RSD alone).

Treatment groups

23 Participants
are divided into 2 treatment groups
Group A: ControlOther 1 intervention
Group B: TestExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

GCF volume

assessment the volume of GCF

Time frame
1 month

Secondary outcomes

1

IL-17

Assessment of IL-17

Time frame
one month

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: