Postoperative Hypersensitivity and Digital Radiographic Assessment of a Zinc Modified Versus a Conventional Glass Ionomer Cement in Deep Carious Lesion: Randomized Controlled Clinical Trial

Carious Dentin Clinical Trial

Official title:

Postoperative Hypersensitivity and Digital Radiographic Assessment of a Zinc Modified Versus a Conventional Glass Ionomer Cement in Deep Carious Lesion: Randomized Controlled Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03285022
• Other study ID #: CEBD-CU-2017-09-17
• Status: Not yet recruiting
• Phase: N/A
• First received: September 14, 2017
• Last updated: September 14, 2017
• Start date: October 20, 2017
• Est. completion date: April 20, 2018

Study information

• Verified date: September 2017
• Source: Cairo University
• Contact: Dina Mounir Elkady, Assitant lecturer
• Phone: 01004297317
• Email: Dina.elkady[@]dentistry.cu.edu.eg
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study aim to evaluate the difference between the effect of zinc modified glass ionomer and conventional glass ionomer on the success of partial caries removel technique

Description:

The zinc ion has an antibacterial effect which could increase the success of partial caries removel technique by decreasing the bactrial population .

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 52
• Est. completion date: April 20, 2018
• Est. primary completion date: April 20, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Male or female (>18 y)

2. patient with At least 1 deep carious lesion

3. Clinical symptoms of reversible pulpitis with positive pulp response

Exclusion Criteria:

• 1. Patient suffer from irreversible pulpitis (pain with hot or instant pain lasting for a while, resistant to analgesic) 2. Presence of any sign of periapical lesion (like sinus tract ) 3. Teeth with periodontal problem 4. Anterior teeth (material used for non aesthetic region) 5. Pregnant women, to avoid multiple exposure to x ray 6. Patients unable to give consent(mentally retarted, or refuse to right a consent)

Related Conditions & MeSH terms

• Carious Dentin
• Dental Caries
• Hypersensitivity

Intervention

Procedure:
• Partial caries removel techniques
Removel of all superfacial dentin and leaving the inner affectted dentin

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Digital radigraphic assessment	The presence of periapical change or change in lamina dura change after the procedure	At baseline ,3months and 6 months
Secondary	Post opreative hypersenstivity	The presence or absence of pain with thermal	Baseline ,at 3 months and at 6 months