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Efficacy of multimodal analgesia before and after impacted mandibular third molar surgery

Not Applicable
Completed
Conditions
Diseases of the digestive system
Registration Number
KCT0005450
Lead Sponsor
Chungnam National University Hospital
Brief Summary

<Efficacy Results> - In Group A, experimental drug significantly reduces pain at 3 and 6 hours after tooth extraction compared to taking a placebo, and also lowers the intensity of the initial perceived pain. - In Group B, experimental drug significantly reduces pain at 1 and 6 hours after tooth extraction compared to taking a placebo, and delays the onset of initial perceived pain. - There is no significant association between the use of experimental drugs and the need for additional analgesics within 12 hours post-surgery in both group A and B. <Safety Results> - There is no significant association between the use of experimental drugs in both group A and B, and the occurrence of adverse reactions (drug-related side effects). - No other abnormal cases were observed in vital signs, physical examinations, or medical procedures.

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
66
Inclusion Criteria

Healthy adult males and females without systemic diseases aged 19 to 40 years old
-Those who have no abnormal findings on blood tests (CBC, aPTT, PT) conducted within the last 3 weeks
-When the impaction of both mandibular third molars is confirmed
-On panoramic radiographs, more than 1/3 of the crown is covered with the alveolar bone and need to be surgically extracted.
(including both gingival incision, tooth separation, bone removal)
-A person who fully understands and agrees with the purpose of the research and voluntarily permits participation in the research

Exclusion Criteria

- Have a history of allergy on drugs used in this study
(Celecoxib, tramadol, acetaminophen, cefaclor, zaltoprofen, rebamipide)
-If there is pericoronitis or benign lesions on the impacted mandibular third molars
- If you need to take the analgesic drugs continuously until the time of extraction and maintains analgesic effect
-Pregnant or lactating person
-Smokers and others who are judged to be inappropriate to participate in clinical trials

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
amount of pain after extraction
Secondary Outcome Measures
NameTimeMethod
occurrence of drug side effect;Time taken from the end of extraction to the first pain and the intensity of the pain at that time
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