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

Phase 2

Completed

• Conditions: the patients with gingivitis; Gingegel Gel gingivitis

• Registration Number: TCTR20220814001
• Lead Sponsor: researchers funding

Brief Summary

A statistically significant enhancement in the clinical parameters for both groups after 2 weeks such as, the reduction of Plaque index (PLI) from (0.967) at baseline of the study to (0.663) after 2 weeks and with mean reductions in Gingival Index (GI) of total sample was (0.994) at baseline of the study reduced to (0.725)after 2 weeks

Detailed Description

Not available

Study Timeline

• Study Completion: 2022-03-01
• Study Start: 2022-08-14
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 50

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

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.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
primary outcome 2 weeks after end of intervention plaque index and gingival index measurment

Secondary Outcome Measures

Name	Time	Method
secondary outcomd 2 weeks after end the intervention gingival index