Preoperative Dose of Co-amoxiclav for Prevention of Postoperative Complications in Dentoalveolar Surgery
Infection
About this trial
This is an interventional treatment trial for Infection focused on measuring dry socket, bleeding, swelling
Eligibility Criteria
Inclusion Criteria:
- Patient age from 16 to 70 yrs old
- Patient needs surgical teeth extraction (subject tooth will be removed using osteotomy by motorised drill).
Exclusion Criteria:
- Patients refusing the preoperative dose of oral co-amoxiclav, and unwilling to take part .
- Patients who are allergic to co-amoxiclve, amoxicillin or metronidazole
- Patient are on warfarin medication
Sites / Locations
- Taibah UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
Active Comparator
Co-Amoxiclav postoperatively alone
Co-Amoxiclav preoperatively with Metronidazole postoperatively
Co-Amoxiclav preoperatively with amoxicillin postoperatively
• Treatment 1: 0.9% normal saline irrigation immediately after the surgery with course of Co-Amoxiclav 625 mg 0.2% chlorhexidine mouthwash following the surgery for 5 days (control group)
• Treatment 2: 625 mg Co-Amoxiclav and 1g Paracetamol preoperatively and 0.2% chlorhexidine mouthwash immediately before the surgery with course of Metronidazole 500 mg and 0.2% chlorhexidine mouthwash following the surgery for 5 days
• Treatment 3: 625 mg Co-Amoxiclav and 1g Paracetamol preoperatively and 0.2% chlorhexidine mouthwash immediately before the surgery with course of amoxicillin 500 mg and 0.2% chlorhexidine mouthwash following the surgery for 5 days