A clinical trail to assess the post operative effects of using ozonated water in dental implant placement procedure.
Phase 3
- Conditions
- Health Condition 1: K084- Partial loss of teeth
- Registration Number
- CTRI/2024/05/067551
- Lead Sponsor
- Krishna Vishwa Vidyapeeth
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
healthy individuals or patients with controlled medical conditions, requiring minimum one dental implant on either side of their upper or lower arches, age 18-75 years, male or female, non-smokers, willingness to sign the informed consent form
Exclusion Criteria
lactating mothers or pregnant women, No bone grafting or augmentation procedures indicated, history of receiving radiotherapy in the head and neck region, patients having mucositis or parafunctional habits, systemically ill patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method decrease in post-operative pain <br/ ><br>faster soft tissue healing around the implantTimepoint: at baseline <br/ ><br>at 48 hours <br/ ><br>at 8 days
- Secondary Outcome Measures
Name Time Method better degree of osseointegrationTimepoint: at 3 months