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Evaluation of Gingegel Gel (0.2% hyaluronic acid) Application in the treatment of gingivitis(Randomize clinical trial

Evaluation of Gingegel Gel (0.2% hyaluronic acid) Application in the treatment of gingivitis(Randomize clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20220814001
Enrollment
50
Registered
2022-08-14
Start date
2021-09-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

the patients with gingivitis Gingegel Gel gingivitis

Interventions

motivation, instruction, scaling, polishing with application of gingegel, and 30 patients , control (motivation, instruction, scaling polishing alone)
Experimental Drug,No Intervention No treatment
gingegel application, control without gingegel application

Sponsors

researchers funding
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 40 Years

Inclusion criteria

Inclusion criteria: Patients who diagnosed as suffering from chronic gingivitis, bleeding while brushing, with minimum 20 remaining teeth except third molars was excluded and willingness to come for follow up visits were included in study subjects with good general and oral health; Subjects who had not received any periodontal therapy for past 3 months; Ability of the subjects to attend the hospital at regular periods

Exclusion criteria

Exclusion criteria: Patients having history of any local and/or systemic antibiotic therapy within previous six months; any immune compro-mised condition or chronic diseases like diabetes; or those receiving radiotherapy or chemotherapy; pregnant and lac-tating females; history of periodontal surgical procedure; patients taking drugs that could affect the condition of the gingival tissues; Subjects undergoing orthodontic treatment; Subjects with muco-gingival problems, pockets and attach-ment loss; Subjects with five or more carious teeth that re-quire immediate treatment; Subjects using any other sup-plemental plaque control measures like interdental cleansing aids or mouthwashes; Subjects with the habit of taking al-cohol, smoking or chewing tobacco; Subjects suffering from any systemic disease; Subjects with chronic desquamative gingivitis.

Design outcomes

Primary

MeasureTime frame
primary outcome 2 weeks after end of intervention plaque index and gingival index measurment

Secondary

MeasureTime frame
secondary outcomd 2 weeks after end the intervention gingival index

Countries

Iraq

Contacts

Public Contactabdulkareem alwan

Dentistry department Alrafidien university college

dr_alsady@yahoo.co.uk07701599576

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026