Status:

UNKNOWN

Rosmarinus Officinalis Versus 2.5%Sodium Hypochlorite as Root Canal Irrigants

Lead Sponsor:

Cairo University

Conditions:

Necrotic Pulp

Eligibility:

All Genders

20-45 years

Phase:

NA

Brief Summary

To measure the Effect of Rosmarinus Officinalis versus 2.5%Sodium Hypochlorite as Root canal Irrigants on the Intensity of post-operative pain and Bacterial Reduction in asymptomatic necrotic Mandibul...

Eligibility Criteria

Inclusion

  • Systematically healthy patient (ASA I and II).
  • Age between 20 and 45 years with no sex predilection
  • Mandibular permanent premolar teeth:
  • Diagnosed clinically with pulp necrosis.
  • Absence of spontaneous pain.
  • Radiographic evidence of root and root canal.
  • Slight widening in the periodontal membrane space or with periapical radiolucency.
  • No response to cold pulp tester (ethyl chloride spray)
  • Patients who can understand and interpret Numerical rating scale (NRS).
  • Patients' acceptance to participate in the trial

Exclusion

  • 1- Medically compromised patients having significant systemic disorders. (ASA III or IV).
  • 2- History of intolerance to NSAIDS. 3- If analgesics or antibiotics have been administrated by the patient during the past 24 hours preoperatively as it might alter their pain perception.
  • 4- Pregnant women: Avoid radiation exposure, anesthesia, and medication. 5- Teeth with: i. Vital teeth. ii. Double canal mandibular premolar teeth iii. Association with swelling or fistulous tract. iv. Acute peri-apical 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.
  • v. Mobility Grade II or III. vi. Pocket depth more than 5mm. vii. Previous root canal therapy. viii. Non-restorable teeth: Hopeless tooth
  • Immature teeth.
  • Radiographic evidence of external or internal root resorption vertical root fracture, perforation, calcification.

Key Trial Info

Start Date :

May 1 2022

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

July 1 2023

Estimated Enrollment :

26 Patients enrolled

Trial Details

Trial ID

NCT05289843

Start Date

May 1 2022

End Date

July 1 2023

Last Update

March 22 2022

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