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The effect of releasing (relaxing) incision on the postoperative complication of mandibular third molar surgery

Phase 2
Conditions
Impacted teeth.
Embedded and impacted teeth
Registration Number
IRCT201506191760N42
Lead Sponsor
Vice Chancellor for Research and Technology, Babol University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
20
Inclusion Criteria

Age range 15-35 years; Mandibular third molar teeth surgery candidates with Pell & Gregory and classified in categories 1 and 2 -A, B
Exclusion criteria:
Smoking;
Taking certain medications such as Corticosteroids or immunosuppressive drugs bisphosphonates; Illnesses such as diabetes, anemia and other debilitating diseases of the immune system; Haemorrhagic disease or taking anticoagulants; Background radiation in head and neck; pericoronitis or any pathological lesions associated with third molars is not growing; Significant injury periosteal flap envelope in

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Complications After Surgery. Timepoint: Daily up to a month after surgery. Method of measurement: Clinical.
Secondary Outcome Measures
NameTimeMethod
Pain Index. Timepoint: Daily up to a month after surgery. Method of measurement: Visual Analogue Scale.;Inflation. Timepoint: On the third, seventh, fourteenth, and one month after surgery. Method of measurement: Clinical.;The Lockjaw. Timepoint: On the third, seventh, fourteenth, and one month after surgery. Method of measurement: Clinical.;Ecchymosis. Timepoint: On the third, seventh, fourteenth, and one month after surgery. Method of measurement: Clinical.;Duration of surgery. Timepoint: Since the start of operation by the end of the last stitch. Method of measurement: Clinical.
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