CTRI/2023/09/058030CompletedPhase 4
Comparative evaluation of efficacy of laser assisted welding and conventional silk sutures for tissue healing after periodontal surgery
Dr. Isha Sridhar1 site in 1 country15 target enrollmentStarted: October 10, 2023Last updated:
Conditions
Trial Snapshot
- Phase
- Phase 4
- Status
- Completed
- Sponsor
- Enrollment
- 15
- Locations
- 1
- Primary Endpoint
- Operative time for wound closure, Wound Healing assessment
Study Overview
Brief Summary
This study is a randomized controlled split mouth clinical trialcomparing the efficacy of laser assisted healing of wounds with the applicationof 20% human albumin and using indocyanine green dye as an adjunct andconventional silk sutures after periodontal flap surgery in chronicperiodontitis patients. The operative time will be measured during theprocedure and clinical parameters will be measured on 3rd , 7thand 14th post operative day.
Study Design
- Study Type
- Interventional
- Allocation
- Computer generated randomization
- Masking
- Open Label
Eligibility Criteria
- Ages
- 20.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Patients with pocket probing depth of more than or equal to 5mm with 4 or more teeth involved in each quadrant after phase 1 therapy with at least 2 quadrants involved, Patients without occlusal discrepancy, Patients without tooth mobility, Motivated patients capable of maintaining oral hygiene on receiving instructions.
Exclusion Criteria
- •Patients with systemic diseases like diabetes, blood disorders, cardiovascular conditions, immunocompromised patients, Patients on immunosuppressants in the last 6 months, Patients with partial denture or orthodontic appliances, Patients allergic to albumin or indocyanine green dye, Smokers.
Outcomes
Primary Outcomes
Operative time for wound closure, Wound Healing assessment
Time Frame: Operative time for wound closure- baseline, Wound healing assessment - baseline, 3rd day, 7th day, 14th day
Secondary Outcomes
- Plaque formation, gingival bleeding, post operative pain assessment(Plaque formation - baseline, 3rd day, 7th day, 14th day)
Investigators
Study Sites (1)
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