Evaluation of the effect of laser on repair and pain caused by surgical crown lengthening
Not Applicable
- Conditions
- surgical crown length.
- Registration Number
- IRCT20110109005570N12
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Systemically healthy patients
From 25 years to 60 years
Patients who have at least two teeth with the need for surgical crown lengthening in different quadrants of the mouth and not adjacent to each other
Exclusion Criteria
Patients with a history of periodontal surgery in the past six months
Uncontrolled systemic disease
Long-term treatment with antibiotics or steroids
poor hygiene
low cooperation
smoking habit
General contraindications for laser therapy
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical signs of re-epithelialization. Timepoint: third and seventh days after surgery. Method of measurement: Observational, 0: there is a distance between the gingival margins, 3: the gingival margins are adjacent, 6: the gingival margin has an overlap.;Clinical signs of inflammation. Timepoint: third and seventh days after surgery. Method of measurement: Observational, 0: redness above 50% of the length of the incision or swelling is visible, 1: redness is seen below 50% 2: redness is not seen.;Clinical signs of haemostasis. Timepoint: third and seventh days after surgery. Method of measurement: Observational, 0. : Bleeding is seen, 1: Fibrin is seen, 2: There is no fibrin.
- Secondary Outcome Measures
Name Time Method Pain at the surgical site. Timepoint: Surgery day, first day, third day. Seventh day after surgery. Method of measurement: visual analog scale.