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Propolis Versus Calcium Hydroxide on Post-Operative Pain in Patients With Necrotic Pulp

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

Post-Operative Pain, Chronic
Necrotic Pulp

Treatments

Dietary Supplement: propolis
Drug: Calcium Hydroxide

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Propolis is a resinous product of honeybees. Propolis is said to be effective against resistant microorganisms inside the root canal compared to the gold standard medication known as calcium hydroxide. The clinical trial tests the effect of propolis versus calcium hydroxide on pain in patients with necrotic teeth.

Full description

Propolis is an immunomodulatory, antioxidant, flavonoid-rich resinous product of honeybees. Propolis was reported as less cytotoxic and more effective against resistant microorganisms than calcium hydroxide as well as biocompatible to the periradicular tissues than existing intracanal medicaments. The aim of this single-blinded randomized clinical trial was to evaluate the effect of propolis versus calcium hydroxide, intracanal medicaments, on post-operative pain in patients with necrotic single canal teeth. Methods: Forty-six participants with an age range of 20-40 years old, diagnosed as having necrotic pulp in their single-rooted, single canal teeth were included in this study, with 23 participants in each group. Treatment was done in two visits and intracanal medicament was applied for one week in between. Participants were instructed to rate their pain score by a numerical rating scale after 24, 48, 72 hours and at 7 days.

Enrollment

46 patients

Sex

All

Ages

20 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • • Asymptomatic patients with age range 20 - 40 years

    • Necrotic, single canal maxillary and mandibular teeth with periapical infection presented as radiolucency or widening in the periodontal membrane space.
    • Medically - free of any systemic disease
    • Teeth with complete root formation

Exclusion criteria

  • • Pregnant or lactating females

    • Teeth with vital pulps, internal or external resorption or anatomic abnormalities
    • Teeth with cracks, curvatures, root caries and calcified canals
    • Double or triple-rooted teeth
    • Patients with facial swelling, acute pulpal or periapical lesion
    • Teeth that are not indicated for endodontic treatment: Bad oral hygiene, mobile or recessed
    • Previously endodontically-treated teeth

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

46 participants in 2 patient groups

Propolis
Experimental group
Description:
intervention intracanal medicament
Treatment:
Dietary Supplement: propolis
Calcium Hudroxide
Active Comparator group
Description:
Gold standard intracanal medicament
Treatment:
Drug: Calcium Hydroxide

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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