Effects of laser on postoperative sensitivity
Phase 2
- Conditions
- Post operative sensitivity.
- Registration Number
- IRCT2012072810425N1
- Lead Sponsor
- Vice chancellor for research, Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 24
Inclusion Criteria
Patients that inform consent before the study began , had at least two cervically lesions without restorations , were free of any painful symptoms , had good health without any systemic disease and good oral hygiene , were free of periodontal disease and without history of periodontal surgery within 3 months.
Patients were excluded from the study if they had mucosal lesion , Had local or systemic drug usage within 2 weeks , Had lichenoid lesions , were pregnant or nursing, had pacemaker and disease which affect treatment
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative sensitivity. Timepoint: 1 day, 2 weeks and 1 month after intervention. Method of measurement: VAS scale.
- Secondary Outcome Measures
Name Time Method