Postoperative Pain After the Removal of Root Canal Fillin... | NCT02905773

Studies
Postoperative Pain After the Removal of Root Canal Filling Material

NCT02905773

Sponsor

TC Erciyes University

Status

Completed

Last Update Posted

Sep 20, 2016Estimated

Enrollment

135Actual

Phase

Early Phase 1

Conditions

Postoperative Pain

Interventions

root canal therapy
root canal retreatment

Countries

Not provided

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Sep 2016

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Mar 2015

Primary Completion Date

May 2016Actual

Completion Date

May 2016Actual

First Submitted Date

Sep 6, 2016

First Submission Date that Met QC Criteria

Sep 14, 2016

First Posted Date

Sep 19, 2016Estimated

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Sep 18, 2016

Last Update Posted Date

Sep 20, 2016Estimated

Description Module

Brief Summary

The aim of this study was to evaluate the intensity and duration of postoperative pain after the removal of root canal filling material in retreatment procedures of upper incisor teeth with chronic apical periodontitis, using different techniques.

The patients were assigned to three groups of 45 patients, according to the method used to remove old canal filling material. The presence of postoperative pain was assessed after 6, 12, 24, 48, and 72 hours, 7 days, and finally after 10 days.

The hypothesis of this study: there would be no difference in postoperative pain intensity among the groups.

Detailed Description

Not provided

Design Module

Study Type

Interventional

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Not provided

Target Follow-Up Duration

Not provided

Phases

Early Phase 1

Interventional Study Design

Allocation

Biospecimen

No data available

No data is available for this block.

Enrollment

135Actual

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
postoperative pain	Other	postoperative pain	Other: root canal therapy
intensity	Other	intensity	Other: root canal retreatment

Interventions

Name	Type	Description	Arm Group Labels	Other Names
root canal therapy	Other	effect of devices ( ProTaper and Reciprocal Files)	postoperative pain

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
postoperative pain after non-surgical endodontic retreatment using modified visual analog scale		10 days

Secondary Outcomes

Not provided

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

asymptomatic incisor teeth with chronic apical periodontitis
patients between 18-55 years of age

Exclusion Criteria:

patients with systemic disease

Accepts Healthy Volunteers

Yes

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

Not provided

Maximum Age

Not provided

Standard Ages

ChildAdultOlder Adult

Study Population

Not provided

Sampling Method

Not provided

Condition Browse Module

MeSH Terms

ID	Term
D010149	Pain, Postoperative

Ancestor Terms

ID	Term
D011183	Postoperative Complications
D010335	Pathologic Processes
D013568	Pathological Conditions, Signs and Symptoms
D010146	Pain

Browse Leaves

Not provided

Browse Branches

Not provided

Intervention Browse Module

MeSH Terms

ID	Term
D012390	Root Canal Therapy

Ancestor Terms

ID	Term
D004708	Endodontics
D003813	Dentistry

Browse Leaves

Not provided

Browse Branches

Not provided