se of oral zinc tablet before third molar surgery
Not Applicable
- Registration Number
- CTRI/2023/06/054150
- Lead Sponsor
- Dr. MAYURI YADAV
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Subjects between 18-50 years
Subjects of both sexes will be included.
Subjects requiring bilateral surgical extraction of mandibular third molars.
Absence of pericoronitis or signs of inflammation
Subjects under category ASA I grade.
Subjects consenting for the study.
Exclusion Criteria
Subjects with an immune-compromised state.
Subjects with a known drug and /or food allergy
Non - cooperative patients, mentally retarded patients.
Pregnant or lactating mothers.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The wound healing is assessed using modified landryâ??s scale on 1,3, and 7th post operative day. The healing index includes five clinical outcome parameters: tissue color (percent of red vs pink gingiva), presence of bleeding on palpation, presence of granulation tissue, incision margin (epithelization and connective tissue exposure), and presence of suppuration. The final score ranged from 0 (poor healing) to 5 (excellent healing).Timepoint: 1,3,7TH POSTOPERATIVE DAY
- Secondary Outcome Measures
Name Time Method PAIN USING VAS SCALETimepoint: 1,3,7TH POSTOEPRATIVE DAY