Effectiveness of Two Intracanal Irrigation Solutions | NCT06427070

Studies
Effectiveness of Two Intracanal Irrigation Solutions

NCT06427070

Sponsor

Misr University for Science and Technology

Status

Unknown status

Last Update Posted

May 23, 2024Actual

Enrollment

1Estimated

Phase

Not Applicable

Conditions

Irreversible Pulpitis

Interventions

Irrigating solution

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

May 2024

Overall Recruitment Status or Expanded Access Status

Unknown status

Last Known Status

Not yet recruiting

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

May 23, 2024Estimated

Primary Completion Date

May 30, 2024Estimated

Completion Date

Jun 1, 2024Estimated

First Submitted Date

May 14, 2024

First Submission Date that Met QC Criteria

May 18, 2024

First Posted Date

May 23, 2024Actual

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

May 18, 2024

Last Update Posted Date

May 23, 2024Actual

Sponsor/Collaborators Module

Responsible Party, by Official Title

Manal Mohamed, Lecturer at Misr university, Misr University for Science and TechnologyPrincipal Investigator

Lead Sponsor

Misr University for Science and TechnologyOTHER

Collaborators

Not provided

Oversight Module

Has Data Monitoring Committee (DMC)

Is FDA Regulated Drug

Is FDA Regulated Device

Is Unapproved Device

Not provided

Pediatric Postmarket Surveillance of a Device Product

Not provided

Product Exported from US

FDAAA801 Violation

Not provided

Description Module

Brief Summary

The aim of the present clinical trial is to investigate and compare the effect of crayotherapy utilizing two intra-canal final irrigating solutions on postoperative pain.

Detailed Description

st: Comparison of pain reduction algorism after cryotherapy using the two tested irrigating materials
nd. Number and frequency of analgesics taken for pain relief during one week postoperative

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

Not Applicable

Interventional Study Design

Allocation

Biospecimen

No data available

No data is available for this block.

Enrollment

1Estimated

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
Irrigating solutions	Experimental	Group 1 sodium hypochlorite Group 2 saline Group 3 chlorohexidine	Other: Irrigating solution

Interventions

Name	Type	Description	Arm Group Labels	Other Names
Irrigating solution	Other	Saline, sodium hypochlorite, chlorohexidine	Irrigating solutions

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
pain scale	pain scale Comparison of the 2 selected irrigating solutions	1 week
Analgesics Frequency	Frequency of analgesics for pain relief	1 week

Secondary Outcomes

Not provided

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Case diagnosed as having symptomatic irreversible pulpitis with symptomatic apical periodontitis
Patients requiring emergency RCT
Pre-operative pain score 7 on Numerical Rating (NRS) scale
Middle aged males (25-50)
Medical profile ASA1
Willing to sign the consent form
Willing to answer our call for one week period

Exclusion Criteria:

Females
Medical conditions above ASA1
Multi-rooted teeth
Patients younger or older than (25-50)

Accepts Healthy Volunteers

Yes

Sex

Male

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

25 Years

Maximum Age

50 Years

Standard Ages

Adult

Study Population

Not provided

Sampling Method

Not provided

Condition Browse Module

MeSH Terms

ID	Term
D011671	Pulpitis

Ancestor Terms

ID	Term
D003788	Dental Pulp Diseases
D014076	Tooth Diseases
D009057	Stomatognathic Diseases

Browse Leaves

Not provided

Browse Branches

Not provided

Intervention Browse Module

MeSH Terms

ID	Term
C049389	dextran - saline drug combination

Ancestor Terms

Not provided

Browse Leaves

Not provided

Browse Branches

Not provided