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A study to compare effect of amoxicillin & clavulinic acid and Moxifloxacin after removal of wisdom tooth.

Phase 4
Conditions
Health Condition 1: K011- Impacted teethHealth Condition 2: null- Impected third molar tooth
Registration Number
CTRI/2019/11/022107
Lead Sponsor
Department of Pharmacology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Age: in between 18 years to 60 years

2. Duration of pain: less than 4 week

3. Participant willing to give written informed consent

4. Participants with impacted mandibular third molar tooth

Exclusion Criteria

1. History of sensitivity to any drugs.

2.H/O Valvular Heart Disease; Bypass surgery within 6 months; on anticoagulant drugs.

3.Pregnant / Lactating women.

4. No written informed consent.

5. BMI < 18.5

6. Uncontrolled Diabetes, Immuno-compromise, on steroid treatment, HIV.

7. Known neuropsychiatric illness.

8. Participants with blood dyscrasia or coagulation disorders.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ocal infectionTimepoint: post operatively on day 0, 1, 3, 5, 7
Secondary Outcome Measures
NameTimeMethod
Post operatively painTimepoint: Post operatively on 2, 4, 6, 24, 72 hours;Swelling, trismus, dysphagia, fever and safety variable during treatment courseTimepoint: post operatively on day 0, 1, 3, 5, 7
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