Overview

Evaluation of the Effect of Systemic Proteolytic Enzyme Therapy.

Status:
Recruiting
Trial end date:
2023-09-30
Target enrollment:
0
Participant gender:
All
Summary
1. To compare the postoperative pain between the patients who receive the systemic enzyme therapy and patients in the control group in the third and seventh day. 2. To compare the postoperative swelling (edema) between the patients who receive the systemic enzyme therapy and patients in the control group in the third and seventh day. 3. To compare the degree of trismus between the patients who receive the systemic enzyme therapy and patients in the control group in the third and seventh day. 4. Measure patients' perceptions of changes in their quality of life in the postoperative period and compare it between the patients who receive the systemic enzyme therapy and patients in the control group in the third and seventh day.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Baghdad
Treatments:
Amoxicillin
Metronidazole
Criteria
Inclusion Criteria:

- Healthy patients over 18 years old of either gender.

- Patients who have impacted mandibular third molar.

- Ability to tolerate surgical procedure.

- Pell and Gregory's classification (Class I and class II, position A and B).

Exclusion Criteria:

- Patients with uncontrolled systemic diseases.

- Patients with history of chemotherapy or radiotherapy therapy to the head and neck
region.

- Acute infection at the surgical site at time of operation.

- The presence of cysts or tumors associated with the impacted teeth.

- Pell and Gregory's classification (class III Position C)