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NCT01878851 Clinical Trial

Characterization of Blood Drawn From the Pulp of Primary Molar Undergoing Pulpotomy or Pulpectomy.

Pulpotomy Clinical Trial

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT01878851
Other study ID # Moti-Kot-HMO-CTIL
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date September 2013
Est. completion date August 2019

Study information
Verified date August 2019
Source Hadassah Medical Organization
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Following medical history and clinical examination the children which are scheduled for treatment with suspected pulpary involved primary teeth will be selected. During the regular treatment if a pulp of primary teeth is opened and before the regular pulpotomy procedure is performed the blood that is flowing out of the pulp will be collected and stored until analyzed for the present of inflammatory markers. Clinical and radiographic evaluation will be obtained in follow up appointments if the child will remain in regular treatments in our clinic.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date August 2019
Est. primary completion date August 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 3 Years to 13 Years
Eligibility Inclusion Criteria:

- Pulpal involved primary teeth with a vital pulp of which a certain amount of blood can be obtained.

Exclusion Criteria:

- systemic disease

- pulp necrosis

- permanent teeth

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Israel Hadassah Medical Organization Jerusalem

Sponsors (1)
Lead Sponsor Collaborator
Hadassah Medical Organization

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Detection of specific inflammatory markers one year
Secondary Pulpotomy failure 1 year
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