Postoperative Pain Associated With Three Endodontic Rotary Systems

Clinical Trial Description

Randomized controlled clinical trial comparing three types of endodontic rotary files to assess their effect on postoperative pain after single visit root canal treatment of premolar teeth diagnosed with acute irreversible pulpitis. ;

Study Design

See also
	Status	Clinical Trial	Phase
	Completed	`NCT03412318` - Evaluation of the Effect of Root Canal Preparation by TF and M-Pro on Post-Operative Pain After Single Visit Endodontic Treatment	N/A
	Completed	`NCT04012424` - The Effect of Premedication With Curcumin on Post-endodontic Pain	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT03412318 - Evaluation of the Effect of Root Canal Preparation by TF and M-Pro on Post-Operative Pain After Single Visit Endodontic Treatment

N/A

Completed

NCT04012424 - The Effect of Premedication With Curcumin on Post-endodontic Pain

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT03065777
Study type	Interventional
Source	Cairo University
Contact	Ola A. Hafez, MD Student
Phone	0021111626076
Email	olahafez2010@hotmail.com
Status	Recruiting
Phase	N/A
Start date	October 2016
Completion date	December 2017

Postoperative Pain Associated With Three Endodontic Rotary Systems

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms