Assessment of Postoperative Pain After Using Various Intracanal Medication in Patients With Necrotic Pulp

• Status: Completed
• Trial end date: 2020-09-18
• Target enrollment: 0
• Participant gender: All

Summary

To assess the Postoperative Pain after using Silver Nanoparticles with and without Calcium Hydroxide as an Intracanal Medication in Patients with necrotic pulp (RCT)

• Phase: Phase 4
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Cairo University
• Treatments: Calcium; Calcium, Dietary

Criteria

Inclusion Criteria:

• Patients who are free from any physical or mental handicapping condition with no underlying systemic disease.

• Non-pregnant females

• Asymptomatic necrotic mandibular single rooted teeth.

• Normal occlusal contact with the opposing teeth.

• Patients accepting to participate in the study.

Exclusion Criteria:

• Medically compromised patients: Pain levels and healing following treatment would be compromised as these patients have shown higher incidence of pain and lower healing rate.

• Pregnant women: Avoid radiation exposure, anesthesia, and medication.

• If analgesics or antibiotics have been administrated by the patient during the past 12 hours preoperatively might alter their pain perception

• Patients reporting bruxism or clenching: Avoid further pressure on an already inflamed tooth inducing subsequent irritation and inflammation Teeth that shows:

• Association with acute periapical abscess and swelling: Need special treatment steps which could involve additional visits with incision and drainage. Also, it could influence initiation and progression of postoperative pain.

• Greater than grade I mobility or pocket depth greater than 5mm. Need special surgical and/or periodontal therapy.

• No restorability: Hopeless tooth.

• Vital teeth

• Immature teeth

• Radiographic evidence of external or internal root resorption.

• Any criterion, not mentioned in the inclusion criteria