Health Condition 1: 8- Other Procedures
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Subjects will be free from any chronic systemic disease, both gender with age range from 15 to 40 years, tooth in question is restorable, permanent necrotic maxillary incisors with incomplete root development without periapical lesions, pulp involvement is either due to caries or trauma and selected teeth have never been subjected to any line of endodontic treatment.
Exclusion criteria
Exclusion criteria: patient show allergic response to ciprofloxacin, metronidazole or minocycline or against any materials which we will use in the study, grossly decayed or fractured teeth that required post and core as final restorations, presence of draining sinus and presence of periodontal pockets, Radiographically, apical foramen less than 1 mm, presence of periapical radiolucency more than 10 mm, presence of external or internal root resorption as well as patients with a history of major surgeries like cardiac, kidney transplantation, haemodialysis, radiographic or clinical identification of ankylosis, root resorption, root fracture, uncooperative patients and legal guardians will not consent to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the incidence and intensity of post-operative pain on VAS with PRF scaffolds, MTA as apical barrier in immature maxillary permanent incisors with necrotic pulp.Timepoint: the incidence and intensity of post-operative pain on VAS with PRF scaffolds, MTA as apical barrier in immature maxillary permanent incisors with necrotic pulp by subjects after 24 hours, 48 hours and 72 hours post operatively. | — |
Secondary
| Measure | Time frame |
|---|---|
| To record the frequency of analgesic intakeTimepoint: by subjects after 24 hours, 48 hours and 72 hours post operatively. | — |
Countries
India
Contacts
post graduate institute of medical education and research