Clinical Trials Logo

Clinical Trial Summary

Recruited patients with immature permanent maxillary anterior teeth with non-vital pulp, and periapical radiolucency, age ranging from 8 to16 years old were randomly allocated into three groups (n=13): Group I, disinfected using the triple antibiotic paste, Group II, disinfection was done using diode laser, and Group III, were disinfected using the triple antibiotic paste, diode laser was used for biostimulation. All groups were evaluated for the increase in root length and thickness and decrease in apical diameter at baseline, 3, 6, 9, and 12 months after treatment


Clinical Trial Description

- The investigator recruited patients who are found eligible to the criteria then randomly allocated into three groups (n=13) - Group I: thirteen teeth were disinfected by triple antibiotic paste then revascularization was done using the blood clot method. - Group II: thirteen teeth were Laser disinfected; revascularization was done using the the blood clot method. - Group III: thirteen teeth were disinfected by triple antibiotic paste then revascularization was done using the the blood clot method followed by diode laser bio-stimulation. - periapical x rays was taken at baseline, 3, 6, 9, and 12 months after treatment for the increase in root length and thickness, decrease in apical diameter evaluation ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05445362
Study type Interventional
Source Minia University
Contact
Status Completed
Phase N/A
Start date February 1, 2019
Completion date February 26, 2021

See also
  Status Clinical Trial Phase
Recruiting NCT05100615 - Healing Assessment of Osseous Defects After Surgical Removal of Periapical Lesions N/A
Completed NCT04607018 - Effect PMA-Zeolite on the Mineral Metabolism and Blood Parameters (MMBP Study) N/A
Completed NCT04761211 - Effect and Safety of Smart Bra (PUMCH) N/A
Recruiting NCT04338633 - Post-operative Pain Reduction N/A
Recruiting NCT04327453 - Effect of Removal of Double Antibiotic Paste on Post Operative Pain N/A
Recruiting NCT04324086 - Effect of Removal of Intracanal Medication on Post Operative Pain N/A