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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02929511
Other study ID # IAH-3
Secondary ID
Status Completed
Phase N/A
First received October 7, 2016
Last updated April 19, 2018
Start date January 1, 2017
Est. completion date April 18, 2018

Study information

Verified date March 2017
Source Isparta Military Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study, the researchers will investigate the effect of single-file reciprocating versus single-file rotational file systems on the postoperative pain in adult patients who have necrotic pulp and apical periodontitis. The participants will be assigned by chance to separate groups that compare 2 different treatments, reciprocating single-file system (Reciproc Blue) and rotational single-file system (OneShape). As a reference, Mtwo multi-file (full-sequence) will be used.


Description:

The infected root canal treatments will be performed using one-visit approach with either a reciprocating single-file system or a continuous rotational single-file system. (Reciproc Blue reciprocating single-file system vs OneShape rotational single-file system). The root canals will be completed in single-visit. The patients will record their postoperative pain during the follow-up period using a VAS scale.


Recruitment information / eligibility

Status Completed
Enrollment 91
Est. completion date April 18, 2018
Est. primary completion date April 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 45 Years
Eligibility Inclusion Criteria:

- Participants who have in their mandibular or maxillary molar teeth necrotic pulp and apical periodontitis.

Exclusion Criteria:

- Pregnancy, drug hypersensitivity, cardiac problems, previously performed endodontics treatment.

Study Design


Intervention

Procedure:
Reciprocating single-file system
The device is moving in CW and CCW direction with different angles. It is a single-file endodontic file. The intervention is Reciproc Blue reciprocating single-file system.
Rotational single-file system.
The device is moving in continuous rotational. It is a single-fie endodontic file.
Active comparator Protaper multi-file system


Locations

Country Name City State
Turkey Askeri Hastane Isparta

Sponsors (1)

Lead Sponsor Collaborator
Isparta Military Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain level A VAS scale will be used for the postoperative pain level. The patients will noted their postoperative pain level according to the VAS scale during the follow-up period. 7 days.
Secondary Analgesic usage The patients will record the consumption of the analgesic during the 7 days of follow-up. 7 days.
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