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Evaluation of the effect of hyaluronic acid on reducing pain after tooth extractio

Phase 1
Conditions
extraction of mandibular molar teeth.
Inflammatory conditions of jaws
M27.2
Registration Number
IRCT20240724062535N1
Lead Sponsor
Islamic Azad University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
17
Inclusion Criteria

Patients aged between 18 and 60 years
Lower molar teeth
bilatral

Exclusion Criteria

Patients with vascular or blood disorders
Users of exogenous corticosteroids and anticoagulants such as aspirin
Patients with a history of asthma and allergies
Patients with uncontrolled systemic disorders
Patients with uncontrolled respiratory, digestive, kidney and lung cardiovascular diseases
Patients with a history of head and neck radiotherapy or chemotherapy, suffering from dry mouth
Pregnant women and nursing mothers
Patients with systemic fungal infections, acute infections and tuberculosis

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The amount of pain. Timepoint: Time intervals of one hour, six hours, twelve hours, twenty-four hours, forty-eight hours, and seventy-two hours after surgical treatment for pain in both control and control sides. Method of measurement: The way to measure pain is based on the VAS criterion.;Maximum mouth opening. Timepoint: Time intervals of one day, three days and seven days after surgical treatment, the amount of maximum mouth opening in millimeters on both control and control sides. Method of measurement: The maximum opening of the mouth is in millimeters and by telephone.
Secondary Outcome Measures
NameTimeMethod
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