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Checking the pain relief and wound healing property of homeopathic medicine after tooth removal

Recruiting
Conditions
Chronic apical periodontitis, (2) ICD-10 Condition: K053||Chronic periodontitis, (3) ICD-10 Condition: K027||Dental root caries, (4) ICD-10 Condition: K006||Disturbances in tooth eruption,
Registration Number
CTRI/2022/11/047476
Lead Sponsor
Dr Anudarsh PK
Brief Summary

The study participants will be selected from patients visiting the Coorg Institute of Dental sciences. 15 – 60 years old Patients who need extraction of teeth in the opposite sides/quadrants of the mouth will be included in the study. The total sample size of 24 will be divided equally and assigned  into two groups namely Group A and Group B. In Group A, participants will be advised to take Arnica Montana 200C globules after first extraction and tablet paracetamol 500 mg after the second extraction in the opposite side of the mouth. In Group B, participants will be advised to take tablet Paracetamol 500 mg after the first extraction and 200C Arnica Montana after the second extraction. Prior to start of procedures written consent will be obtained from the participants. The extracted site will be evaluated on the 3rd and 7th day postoperatively for assessment of pain and wound healing. Second extraction in the opposite side of the mouth will be done after 7 days from the first extraction. The extracted site will be evaluated on the 3rd and 7th day postoperatively for assessment of pain and wound healing. Pain will be assessed using 4-point verbal rating scale and wound healing will be assessed by examining the extracted site for signs ofnormal healing alveolus, acutely inflamed alveolus, acutely infected alveolus, alveolar osteitis.

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
All
Target Recruitment
24
Inclusion Criteria
  • 1)Individuals who are willing to participate in the study.
  • 2)Individuals who needs extraction of teeth in the opposite quadrants.
Exclusion Criteria
  • 1)Individuals with severe dental infection.
  • 2)Individuals who are in antibiotic treatment 3)Individuals with uncontrolled diabetes 4)Individuals with any bleeding or clotting disorders.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
A 4-point verbal rating scale (VRS) questionnaire will be used for the assessment of pain.IT WILL BE CHECKED AT THE 3RD AND 7TH DAY AFTER EXTRACTION OF EACH TOOTH.
Secondary Outcome Measures
NameTimeMethod
Wound healing, will be assessed by evaluating the extracted site for signs of normal healing alveolus, acutely inflamed alveolus, acutely infected alveolus, alveolar osteitis.IT WILL BE CHECKED AT THE 3RD DAY AND 7TH DAY AFTER THE EXTRACTION OF EACH TOOTH.

Trial Locations

Locations (1)

COORG INSTITUTE OF DENTAL SCIENCES

🇮🇳

Kodagu, KARNATAKA, India

COORG INSTITUTE OF DENTAL SCIENCES
🇮🇳Kodagu, KARNATAKA, India
Dr JITHESH JAIN
Principal investigator
9448706263
drjitheshjain@yahoo.co.in

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