None listed
Conditions
Interventions
Intervention1: group(1) ciprofloxacin coated suture material: 3 months
Control Intervention1: group(2) pomade coated suture material: 3 months
Control Intervention2: group(3) uncoated silk suture mate
Sponsors
Panineeya mahavidhyalaya institute of dental sciences
Eligibility
Inclusion criteria
Inclusion criteria: patients in the age-group of 18–45 years. Stage II grade B periodontitis. No antimicrobial therapy prior to 3 months.
Exclusion criteria
Exclusion criteria: Patients suffering from systemic illness. Pregnant women. Lactating women. Patients allergic to ciprofloxacin, iodoform and calendula oil. Smokers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Whether ciprofloxacin coated suture material is superior to pomade coated suture materialTimepoint: base line and one week | — |
Secondary
| Measure | Time frame |
|---|---|
| Timepoint: | — |
Countries
India
Contacts
Public ContactRACHAKONDA KAVYA
panineeya mahavidhyalaya institute of dental sciences and research centre
Outcome results
None listed