Status:
NOT_YET_RECRUITING
Clinical and Radiographic Evaluation of Zinc Oxide-Propolis Mixture Versus Modified Triple Antibiotic Paste in LSTR
Lead Sponsor:
Cairo University
Conditions:
Pain, Postoperative
Periapical; Infection
Eligibility:
All Genders
4-7 years
Phase:
NA
Brief Summary
The aim of this study is to evaluate and compare the clinical effectiveness of zinc oxide-propolis mixture with triple antibiotic paste in LSTR as root canal filling material in necrotic primary molar...
Detailed Description
The promising results of propolis as a natural antibiotic in previous in- vivo studies made it interesting to combine propolis to the golden standard zinc oxide eugenol as an intracanal medication in ...
Eligibility Criteria
Inclusion
- Children:
- Cooperative children aged 4 -7 years old.
- Systemically healthy.
- Teeth:
- Clinical criteria:
- Necrotic primary mandibular second molar teeth.
- Spontaneous pain or tenderness to percussion
- Deep carious lesion with pulp exposure.
- Presence of chronic apical abscess or sinus tract Tooth should be restorable. (Thakur et al., 2021)
- Radiographic criteria:
- Coronal-radiographic evidence of a deep carious lesions or lesion approximating pulp
- Radicular discontinuity of lamina dura, furcation involvement less than or equal to half of shortest root in vertical dimension. (Thakur et al., 2021)
Exclusion
- Children:
- With physical or emotional alteration.
- Children with systemic disease.
- Previous history of allergy to antibiotics used in the study.
- Children that will not attend follow up. • Teeth:
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- Non restorable carious primary molars.
- Grade III mobility
Key Trial Info
Start Date :
March 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
January 31 2025
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT06158451
Start Date
March 1 2024
End Date
January 31 2025
Last Update
February 7 2024
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