Acidity Level of Blood From Primary Molar's Pulp While Undergoing Pulpotomy or Pulpectomy Procedure
This study is currently recruiting participants.
Verified July 2012 by Hadassah Medical Organization
Sponsor:
Hadassah Medical Organization
Information provided by (Responsible Party):
Moti Moskovitz, Hadassah Medical Organization
ClinicalTrials.gov Identifier:
NCT01486537
First received: December 3, 2011
Last updated: July 19, 2012
Last verified: July 2012
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Purpose
The aim of this study is to evaluate the level of acidity of blood samples that are been taken from pulp chambers of primary molars undergoing pulpotomy or pulpectomy procedures. Our hypothesis is that samples from teeth undergoing pulpectomy would be acidic while samples from teeth undergoing pulpotomy would bo neutral.
| Condition |
|---|
|
Healthy |
| Study Type: | Observational |
| Study Design: | Time Perspective: Prospective |
| Official Title: | Characterization of Blood Drawn From the Pulp of Primary Molar Undergoing Pulpotomy or Pulpectomy. |
Resource links provided by NLM:
Further study details as provided by Hadassah Medical Organization:
Biospecimen Retention: None Retained
Detailed Description:
blood specimens which are undergoing Astrop test (acidity level .po2 pco2)
| Estimated Enrollment: | 50 |
| Study Start Date: | December 2011 |
| Estimated Primary Completion Date: | December 2012 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
| theeth undergoing pulpotomy |
| teeth undergoing pulpectomy |
Detailed Description:
The samples will be collected by 1 m"l syringe that is pre-washed with Heparin.than the samples will be analyzed in an Astrop machine of neonates.
Eligibility| Ages Eligible for Study: | 3 Years to 13 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Study Population
healthy children undergoing dental treatment by residents in Hadassah hospital Jerusalem.
Ages between 3-13 years old.
Criteria
Inclusion Criteria:
- no systemic disease
- teeth that are undergoing pulpotomy or pulpectomy
Exclusion Criteria:
- systemic disease
- pulp necrosis
- permanent teeth
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01486537
Contacts
| Contact: Moti Moskovitz, DMD, PhD | 00 972 2 6778496 | motim@md.huji.ac.il |
Locations
| Israel | |
| Hadassah Medical Organization, Jerusalem, Israel | Recruiting |
| Jerusalem, Israel, 91120 | |
| Contact: Arik Tzukert, DMD 00 972 2 6776095 arik@hadassah.org.il | |
| Contact: Hadas Lemberg, PhD 00 972 2 6777572 lhadas@hadassah.org.il | |
| Principal Investigator: Moti Moskovitz, DMD, PhD | |
Sponsors and Collaborators
Hadassah Medical Organization
Investigators
| Principal Investigator: | Moti Moskovitz, Dr. | Hadassah Medical Organization |
More Information
No publications provided
| Responsible Party: | Moti Moskovitz, dr, Hadassah Medical Organization |
| ClinicalTrials.gov Identifier: | NCT01486537 History of Changes |
| Other Study ID Numbers: | pulpastrop-HMO-CTIL |
| Study First Received: | December 3, 2011 |
| Last Updated: | July 19, 2012 |
| Health Authority: | Israel: Ministry of Health |
Keywords provided by Hadassah Medical Organization:
|
samples children the age group 3-13 years |
ClinicalTrials.gov processed this record on May 19, 2013