Investigating the hemostatic effect of a surgical hemostat sponge

Not Applicable

• Conditions: Extraction of the first and second mandibular teeth.; Alveolitis of jaws; M27.3

• Registration Number: IRCT20200919048756N8
• Lead Sponsor: Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 27 May 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Need for extraction of two mandibular first molars
Age between 20-45 years
No corticosteroids and antibiotics using in the last month
No coagulation disorders
No acute or uncontrolled infection at the dental surgery site
No malignancy at the dental surgery site
No site exposure Radiation surgery
No contraceptives using at last month
No smoking
No hypertension, diabetes, thyroid disorders and blood diseases

Exclusion Criteria

People taking anticoagulants
Not signing the consent form
Having a systemic disease
Patients whose teeth do not come out normally and need surgery and sectioning

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Blood clotting. Timepoint: The amount of bleeding will be recorded after the anesthesia is gone (within 1-4 hours after tooth extraction) and the amount of uncontrollable bleeding after 4 hours will be considered as active bleeding. Method of measurement: In the study groups, sterile gas is changed every 15 minutes to completely stop the bleeding. The difference in weight of sterile gauze at the beginning and after blood absorption will indicate the amount of blood absorption of each sterile gauze. The number of sterile gauzes consumed and the total weight of sterile blood gauzes absorbed in each group (test and control) will be compared.