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NCT03032978 Clinical Trial

Calcium Silicate Versus Calcium Hydroxide in Two-step Indirect Pulp Treatment

Deep Caries Clinical Trial

Official title:
Clinical and Microbiological Evaluation of Calcium Silicate Versus Calcium Hydroxide in Two-step Indirect Pulp Treatment: Randomized Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03032978
Other study ID # CEBD-CU-2017-01-06
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 20, 2018
Est. completion date May 15, 2019

Study information
Verified date January 2020
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Clinical and microbiological evaluation of Calcium silicate versus Calcium hydroxide in two-step indirect pulp treatment: Randomized clinical trial

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date May 15, 2019
Est. primary completion date March 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- 18-50 years.

- Males or females.

- Co-operative patients approving to participate in the trial.

Exclusion Criteria:

- Patients younger than 19 years old or older than 50 years old.

- Disabilities.

- Systemic diseases or severe medically compromised.

- Lack of compliance.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Calcium hydroxide
Pulp capping material
• Calcium silicate
Pulp capping material

Locations
Country Name City State
Egypt Ehsan Hossam Cairo Giza Governorate

Sponsors (1)
Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain: VAS post operative pain after 6 month from material application will be measured by visual analogue scale (VAS)with score from 0 to 10 in which 0 means no pain and 10 means the worst pain 6 month
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