Clinical Trials Logo

Clinical Trial Summary

Recruited patients with necrotic pulp after application of Calcium hydroxide are assigned to group (XP Endo Finisher file) and group( Passive ultrasonic irrigation) and group (conventional syringe irrigation with side vented needle) to remove intracanal medication and record postoperative pain afterwards.


Clinical Trial Description

The investigator will recruit patients who are found eligible to the criteria, Calcium hydroxide will be inserted inside the canals. After 7 days, patients will be randomly assigned to either removal of intracanal medication using, the XP-Endo Finisher file, passive ultrasonic irrigation (PUI) and conventional syringe irrigation with side vented needle.

After the visit, patients will be asked to record post operative pain by Visual Analog Scale)in a given sheet ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04324086
Study type Interventional
Source Minia University
Contact Shaimaa Nasr El-din Abd El-Ghaffar, PHD
Phone +0201020271788
Email dr_shimes@hotmail.com
Status Recruiting
Phase N/A
Start date April 1, 2020
Completion date October 1, 2020

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 NCT05445362 - Efficacy of Diode Laser in Maturogenesis of Immature Teeth With Necrotic Pulps N/A
Completed NCT04761211 - Effect and Safety of Smart Bra (PUMCH) N/A
Recruiting NCT04327453 - Effect of Removal of Double Antibiotic Paste on Post Operative Pain N/A
Recruiting NCT04338633 - Post-operative Pain Reduction N/A