Comparison of two blood products in healing of extraction sockets - A split mouth randomized clinical trial
Not Applicable
- Conditions
- Health Condition 1: K011- Impacted teeth
- Registration Number
- CTRI/2021/01/030564
- Lead Sponsor
- Sanchit Mahajan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Subject requiring surgical removal of bilateral impacted mandibular third molars.
2.Subject requiring surgical removal of Soft tissue impacted mandibular third molar
3.Subjects who are in good physical health with no clinically significant and relevant
4.No medical history.
5.Subject who understood and are willing to follow with all study procedure.
Exclusion Criteria
1.Subject requiring surgical removal of unilateral impacted mandibular third molars
2.Subject unable or unwilling to sign the informed consent form.
3.Immunocompromised individuals including those with severe debilitating diseases.
4.Pregnant, lactating or female subjects taking oral contraceptive were not included.
5.Patients who are smokers will be excluded from the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method comparison of bone density will be done on both sides using a cone beam computed tomographyTimepoint: at 6 months
- Secondary Outcome Measures
Name Time Method post operative pain and swelling on either side will be measuredTimepoint: pain and swelling will be measured on 1st 3rd and 7th post op day