Endoscopic Treatment During Endodontic Procedures

The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2011 by Barzilai Medical Center.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Barzilai Medical Center
ClinicalTrials.gov Identifier:
NCT01192607
First received: August 31, 2010
Last updated: March 1, 2011
Last verified: March 2011

August 31, 2010
March 1, 2011
April 2007
November 2007   (final data collection date for primary outcome measure)
Endoscopic root canal treatment [ Time Frame: 1 month ] [ Designated as safety issue: Yes ]
Same as current
Complete list of historical versions of study NCT01192607 on ClinicalTrials.gov Archive Site
Endoscopic root canal complications [ Time Frame: 1 month ] [ Designated as safety issue: Yes ]
Same as current
Not Provided
Not Provided
 
Endoscopic Treatment During Endodontic Procedures
Endoscopic Treatment During Endodontic Procedures

The objectives of this Phase I study is to evaluate the safety and effectiveness of the endoscopic endodontic equipment device for root canal assistance treatment as well as to evaluate the ease of use of this device, by a surgeon experienced in endodontic treatment, in a true clinical setting.

This open, phase 1 trial will be conducted on 15 patients with the need for root canal treatment. The teeth will be permanent teeth in which the need for root canal treatment was decided by his dentist in the dental clinic in the Barzilai medical center Ashkelon. Videoendoscopy of the procedure will be recorded and will include a post-op view of the treatment. Patients will be followed up for pain infection and any potential complications; immediately, at 4 weeks 12 weeks and 6 month post- op. The procedure will also be taped externally to document surgeon's convenience with the equipment.

The procedures will be performed under local or general anesthesia in an ambulatory environment, using standard root canal equipment, which will include endodontic hand and rotary files, endodonically used irrigating solutions and the videoendoscopy equipment. Under this protocol the basic treatment will be carried out by professional well trained endodontist in the same way used for root canal treatment. Following the mechanical preparation of the canal the endoscope, connected to a video camera and monitor, is introduced with the help of isotonic saline irrigation. With the aid of the endoscope remains of soft tissue from the pulp tissue will be coagulated with the ERBOTOM ICC 80 monopolar fibers and removed with the irrigation, the canal will be inspected for lateral canals and the monoplar fibers will be used for coagulating and removal of this tissue. Er-Yag laser fiber connected to Erbium laser generator will be used for finalizing the canal preparation and preparation of the lateral canals. Actual lasing and coagulation will be performed only under clear vision, when the fiber is seen to be in direct contact with the tissue. Adequate irrigation will be maintained throughout the procedure using an intravenous bag connected to the irrigation port on the sheath of the endoscope.

The endoscope device will be connected to the Erbbe diathermy ERBOTOM ICC 80 for coagulation monopolar fibers 0.05-0.1 mm number 20197-021-022 .

Standard Lumenis Opus 20, dental Erbium:YAG laser available in the hospital. Lasing will begin at a setting of 300 mj per pulse and a pulse rate of 7 Hz.

The same procedures performed on 15 human teeth in a lab status. The insertion of the instruments to the root canal will be in 2 techniques:1) Via the endoscope channel and 2) The instruments will be inserted parallel to the endoscope.

Interventional
Phase 1
Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Dental Pulp Cavity
  • Root Canal Treatment
  • Endoscopy
Device: Endoscopic treatment during root canal treatment
Endoscopic treatment during root canal treatment
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
15
December 2011
November 2007   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Over 18 years old
  2. Suffers from deep carries, acute or chronic pulpitis crown fracture which root canal treatment is the treatment of choice.
  3. Patient understands and has signed the Informed Consent Form.

Exclusion Criteria:

  1. Teeth with cracks or root fracture.
  2. Patients on anti-coagulants.
  3. Patients with cardiac diseases, kidney insufficiency, any malignancy or any steroid therapy.
Both
18 Years and older
Yes
Contact: Oded Nahlieli, DMD 972 524351116 nahlieli@yahoo.com
Israel
 
NCT01192607
HTA3741, BAR1404CTIL
No
oded nahlieli, OMFS BARZILAI MEDICAL CENTER
Barzilai Medical Center
Not Provided
Principal Investigator: Oded Nahlieli, DMD Barzilai Medical Center
Barzilai Medical Center
March 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP