NCT01486537

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
87

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Dec 2011

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2011

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

December 3, 2011

Completed
3 days until next milestone

First Posted

Study publicly available on registry

December 6, 2011

Completed
8.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2020

Completed
Last Updated

March 16, 2022

Status Verified

March 1, 2022

Enrollment Period

8.9 years

First QC Date

December 3, 2011

Last Update Submit

March 14, 2022

Conditions

Healthy

Keywords

sampleschildrenthe age group 3-13 years

Study Arms (2)

theeth undergoing pulpotomy

teeth undergoing pulpectomy

Eligibility Criteria

Age3 Years - 13 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)
Sampling MethodNon-Probability Sample
Study Population

healthy children undergoing dental treatment by residents in Hadassah hospital Jerusalem. Ages between 3-13 years old.

You may qualify if:

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

You may not qualify if:

  • systemic disease
  • pulp necrosis
  • permanent teeth

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hadassah Medical Organization, Jerusalem, Israel

Jerusalem, 91120, Israel

Location

Biospecimen

Retention: NONE RETAINED

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

Study Officials

  • Moti Moskovitz, Dr.

    Hadassah Medical Organization

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
dr

Study Record Dates

First Submitted

December 3, 2011

First Posted

December 6, 2011

Study Start

December 1, 2011

Primary Completion

November 1, 2020

Study Completion

November 1, 2020

Last Updated

March 16, 2022

Record last verified: 2022-03

Locations

IL(1)