SOFT TISSUE CHANGES AND BONE LEVELS AROUND DENTAL IMPLANTS WITH LASER
- Conditions
- Disorder of gingiva and edentulousalveolar ridge, unspecified,
- Registration Number
- CTRI/2022/06/043270
- Lead Sponsor
- Dr YNR SUDESHNA TULABANDULA
- Brief Summary
The procedure will be performed under local anesthesia using 2% lignocaine containing adrenaline 1:80,000.
Implants will be placed by following surgical procedure in both the groups.
After adequate local anesthesia, a mid-crestal incision is given in both the cases. A mucoperiosteal flap is elevated and bone will be exposed.
Selected size of implants (3.5mm and 10mm) will be placed in group I and group II sites.
The implant site will be prepared with standard drills. The osteotomy site is prepared with sequence of drills to the size of implant.
Sites in group I will be treated with Low Level Laser and group II sites will not be treated with Low Level Laser.
Flaps will be approximated and sutured. Instructions regarding oral hygiene maintenance and soft diet plan will be provided. Patient will be discharged after prescribing analgesics and antibiotic. Patient is recalled after 1 week for suture removal. Crown placement will be done after 3 months.clinical parameters like thickness of keratinized tissue, modified gingival index, modified plaque index, width of the keratinized tissue and crestal bone level (by IOPA radiographs) will be assessed at baseline, 3 months and 6 months.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 20
- 1.Individuals in need of tooth replacement.
- 2.Presence of adequate keratinized mucosa in the edentulous site.
- 3.Apparently healthy individuals.
- 4.Isolated mandibular edentulous sites with adequate bone quality and volume with D2 and D3 type of bone.
- 5.Individuals with age group of 20-60 years of either gender .
- 6.Patients who are willing to give informed consent.
- 1.Smokers 2.Individuals with parafunctional habits.
- 3.Pregnant and lactating women.
- 4.Systemic diseases that contraindicate implant placement and surgical procedure.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 2. To evaluate the peri implant crestal bone levels and soft tissue changes without Low level laser therapy. baseline, 7th day, 6 weeks, 3 months and 6 months after implant placement 1. To evaluate the peri implant crestal bone levels and soft tissue changes with Low level laser therapy. baseline, 7th day, 6 weeks, 3 months and 6 months after implant placement
- Secondary Outcome Measures
Name Time Method To compare the soft tissue changes and peri implant crestal bone levels with and without Low level laser therapy.
Trial Locations
- Locations (1)
sibar institute of dental sciences-guntur
🇮🇳Guntur, ANDHRA PRADESH, India
sibar institute of dental sciences-guntur🇮🇳Guntur, ANDHRA PRADESH, IndiaDr YNR SUDESHNA TULABANDULAPrincipal investigator8008013885tsudeshna13@gmail.com