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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06193720
Other study ID # XFMD126
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 3, 2022
Est. completion date August 20, 2023

Study information

Verified date December 2023
Source Saint-Joseph University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Aim: The aim of this study is to evaluate the action of the homeopathic plant Arnica Montana on postoperative edema, pain and trismus after surgical extraction of impacted wisdom teeth. 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.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date August 20, 2023
Est. primary completion date August 20, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 16 Years to 40 Years
Eligibility Inclusion Criteria: - Symmetrically impacted bilateral third molars (mandibular or maxillary). - 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: - Not symmetrically impacted third molars - Patients with health problems

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Arnica montana
Assess the effect of arnica montana on pain, swelling ans trismus after impacted third molar surgery
Other:
Placebo
Patients will take placebo drug after surgeries

Locations

Country Name City State
Lebanon Saint Joseph University Beirut

Sponsors (1)

Lead Sponsor Collaborator
Saint-Joseph University

Country where clinical trial is conducted

Lebanon, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain VSA Assessment of pain on visual analogue scale (between 0 and 10, 0 being no pain at all and 10 being the worst pain) at 0,1,2,3,4,5,6,7 days after surgery
Primary Amount of face Swelling Assessment of swelling after the intervention using a flexible ruler to measure the distance between fixed fixed reference points marked on the face:
G: Mandibular angle
C: External canthus
T: Tragus
S: Sub-nasal point
P: Pogonion
at 0,2,7 days after surgery
Primary Trismus intensity Assessment of limitation of mouth opening after intervention between the incisal edges of the maxillary and the mandibular central incisors using a vernier caliper at 0,2 and 7 days after surgery
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