Trial record 8 of 17 for:    Open Studies | "Heartburn"

Acidity Level of Blood From Primary Molar's Pulp While Undergoing Pulpotomy or Pulpectomy Procedure

This study is currently recruiting participants. (see Contacts and Locations)
Verified August 2015 by Hadassah Medical Organization
Information provided by (Responsible Party):
Moti Moskovitz, Hadassah Medical Organization Identifier:
First received: December 3, 2011
Last updated: August 18, 2015
Last verified: August 2015
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.


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
blood specimens which are undergoing Astrop test (acidity level .po2 pco2)

Estimated Enrollment: 50
Study Start Date: December 2011
Estimated Primary Completion Date: December 2016 (Final data collection date for primary outcome measure)
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.

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.


Inclusion Criteria:

  • no systemic disease
  • teeth that are undergoing pulpotomy or pulpectomy

Exclusion Criteria:

  • systemic disease
  • pulp necrosis
  • permanent teeth
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01486537

Contact: Moti Moskovitz, DMD, PhD 00 972 2 6778496

Hadassah Medical Organization, Jerusalem, Israel Recruiting
Jerusalem, Israel, 91120
Contact: Arik Tzukert, DMD    00 972 2 6776095   
Contact: Hadas Lemberg, PhD    00 972 2 6777572   
Principal Investigator: Moti Moskovitz, DMD, PhD         
Sponsors and Collaborators
Hadassah Medical Organization
Principal Investigator: Moti Moskovitz, Dr. Hadassah Medical Organization
  More Information

No publications provided

Responsible Party: Moti Moskovitz, dr, Hadassah Medical Organization Identifier: NCT01486537     History of Changes
Other Study ID Numbers: pulpastrop-HMO-CTIL
Study First Received: December 3, 2011
Last Updated: August 18, 2015
Health Authority: Israel: Ministry of Health

Keywords provided by Hadassah Medical Organization:
the age group 3-13 years processed this record on November 25, 2015