MedTrace Logo

Electrical and Formocresol Pulpotomy in Primary Molars

NCT01622153 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2017-05-10

No results posted yet for this study

Summary

1. The investigator hypothesize that the Laser pulpotomy will provide adequate and comparable success clinically in primary molars.
2. The investigators hypothesize that the Laser pulpotomy will provide adequate and comparable success radiographically in primary molars.

Conditions

  • Reversible Pulpitis
  • Caries

Interventions

PROCEDURE

Formocresol application after pulpotomy preparation

1:5 Buckley's Formocresol dilution applied for 5 minutes or until hemostasis achieved

PROCEDURE

GENTLEray 980 Soft Tissue diode laser

Application to pulp chamber until hemostasis achieved

Sponsors & Collaborators

  • University Hospitals Cleveland Medical Center

    lead OTHER

Principal Investigators

  • Gerald A Ferretti, DDS, MS, MPH · University Hospitals Cleveland Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
3 Years
Max Age
8 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-06-30
Primary Completion
2014-06-30
Completion
2014-06-30

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01622153 on ClinicalTrials.gov