The Impact of Arnica Montana Following the Surgical Extraction of Impacted Third Molars
NCT ID: NCT06193720
Last Updated: 2024-01-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
10 participants
INTERVENTIONAL
2022-02-03
2023-08-20
Brief Summary
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Materials and Methods: The study is a double-blinded clinical trial recruiting patients undergoing surgical extraction of symmetrically impacted maxillary or mandibular third molars (right and left side). Patients receive alternately and randomly the verum (Arnica Montana 12 CH) or the placebo, in the form of capsules, to be taken 1 day prior to surgery and for 7 days postoperatively. Clinical parameters are collected and include: pain score, maximum mouth opening and facial measurements to assess edema's intensity.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Arnica Montana
Patients will take Arnica montana before and after surgery
Arnica montana
Assess the effect of arnica montana on pain, swelling ans trismus after impacted third molar surgery
Control
Patients will take placebo pills to compare the results
Placebo
Patients will take placebo drug after surgeries
Interventions
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Arnica montana
Assess the effect of arnica montana on pain, swelling ans trismus after impacted third molar surgery
Placebo
Patients will take placebo drug after surgeries
Eligibility Criteria
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Inclusion Criteria
* Young patients aged between 16 and 40 years old.
* No consumption of tobacco or coffee.
* Consent to the terms and conditions of the study.
* Good oral hygiene.
* ASA 1.
Exclusion Criteria
* Patients with health problems
16 Years
40 Years
ALL
Yes
Sponsors
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Saint-Joseph University
OTHER
Responsible Party
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Christian Makary
Professor
Locations
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Saint Joseph University
Beirut, , Lebanon
Countries
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Other Identifiers
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XFMD126
Identifier Type: -
Identifier Source: org_study_id
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