Diplen LX membrane and Coe-pack usage from the patient preference point of view and on the pain and wound healing
Phase 3
Recruiting
- Conditions
- Pain after surgery.Pain, not elsewhere classified
- Registration Number
- IRCT20100412003690N10
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 26
Inclusion Criteria
Moderate to severe periodontitis
Consent to participate in the study
Under 20 percents plaque index
Depth of probing envelope greater than 5 mm
Exclusion Criteria
Pregnant and lactating women
Smokers
Minor peridontitis
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain after surgery. Timepoint: 3, 7 and 14 days after intervention. Method of measurement: Visual Analogue Scale.;Wound healing after surgery. Timepoint: 7 and 14 days after intervention. Method of measurement: Wound healing index.
- Secondary Outcome Measures
Name Time Method