Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
40 participants
INTERVENTIONAL
2022-07-01
2023-07-22
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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oral hygiene instructions and SRP of all teeth plus placebo gel.
SRP of all teeth
Patients received oral hygiene instructions and SRP of all teeth.
oral hygiene instructions and SRP of all teeth, followed by insertion of the spirulina gel.
spirulina gel
Patient were received spirulina gel in diseased sites. The process will be repeated at 7, 14, 21 days.
SRP of all teeth
Patients received oral hygiene instructions and SRP of all teeth.
Interventions
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spirulina gel
Patient were received spirulina gel in diseased sites. The process will be repeated at 7, 14, 21 days.
SRP of all teeth
Patients received oral hygiene instructions and SRP of all teeth.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Pregnant, postmenopausal women. ·
* People who take anti-inflammatory drugs, antibiotics, or vitamins within the previous 3 month.
* People who use mouth washes regularly ·
* Participation in other clinical trials.
35 Years
50 Years
ALL
No
Sponsors
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Kafrelsheikh University
OTHER
Responsible Party
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Enas Elgendy
Prof. of Oral Medicine and Periodontology
Locations
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Kafrelsheikh University
Tanta, , Egypt
Countries
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Other Identifiers
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5
Identifier Type: -
Identifier Source: org_study_id
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