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Comparison of the effect of bromoline drug on pain and trismus after dental surgery

Phase 1
Conditions
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Registration Number
IRCT20230131057290N1
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
80
Inclusion Criteria

Needing mandibular third molar surgery
Age between 17-35 years
Semi-embedded mesiangular mandibular third molar teeth

Exclusion Criteria

Patients who have taken painkillers or other drugs within 24 hours before surgery.
have a history of addiction to drugs or painkillers
Patients who are pregnant or breastfeeding, or have a known sensitivity to analgesics, common non-steroidal anti-inflammatories or cyclooxygenase-2 inhibitors.
Those who have a history of nasal polyps, bronchospasm or angioedema caused by non-steroidal anti-inflammatories.
Patients who were not able to take medicine orally

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: 1, 3 and 7 days after surgery. Method of measurement: A visual analogue scale (VAS), with 10 points, will be evaluated from 0 for no pain to 10 for worst possible pain.;Trismus. Timepoint: 1, 3 and 7 days after surgery. Method of measurement: The degree of trismus is also measured by measuring the inter-incisal distance using a measuring caliper and the results are reported with an accuracy of 0.01 mm.
Secondary Outcome Measures
NameTimeMethod
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