Status:

UNKNOWN

Effect of Etidronate in Sodium Hypochlorite Versus Sodium Hypochlorite on the Intensity of Postoperative Pain

Lead Sponsor:

Cairo University

Conditions:

Necrotic Pulp

Eligibility:

All Genders

18-50 years

Phase:

NA

Brief Summary

To compare the effect of using Etidronate in sodium hypochlorite versus sodium hypochlorite irrigating solution on: * Postoperative pain in patients with necrotic pulp. * Bacterial load reduction \& ...

Detailed Description

Patients will be clinically and radiographically examined and their eligibility will be assessed Eligible patients will be treated in 2 visits 1. Anesthetizing the tooth using inferior alveolar nerve...

Eligibility Criteria

Inclusion

  • Patients who are free from any physical or mental handicapping condition with no underlying systemic disease.
  • Mandibular permanent premolar teeth:
  • Diagnosed clinically with pulp necrosis.
  • Absence of spontaneous pain
  • Slight widening in the periodontal membrane space or with a periapical radiolucency
  • Patients' acceptance to participate in the trial.
  • Patients who can understand pain scale and can sign the informed consent

Exclusion

  • 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 24 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 5 mm. Need special surgical and/or periodontal therapy.
  • Hopeless tooth.
  • Vital teeth.
  • Immature teeth.
  • Radiographic evidence of external or internal root resorption vertical root fracture, perforation, calcification.

Key Trial Info

Start Date :

September 1 2019

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

September 1 2021

Estimated Enrollment :

34 Patients enrolled

Trial Details

Trial ID

NCT04035330

Start Date

September 1 2019

End Date

September 1 2021

Last Update

July 29 2019

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