Effectiveness of Two Intracanal Irrigation Solutions

May 18, 2024 updated by: Manal Mohamed, Misr University for Science and Technology

Effectiveness of Two Intracanal Irrigation Solutions Delivered Through Cryotherapy on Post-Endodontic Pain Relieve. A Randomized Clinical Trial

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.

Study Overview

Status

Not yet recruiting

Intervention / Treatment

Detailed Description

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

Study Type

Interventional

Enrollment (Estimated)

1

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

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)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Irrigating solutions
Group 1 sodium hypochlorite Group 2 saline Group 3 chlorohexidine
Saline, sodium hypochlorite, chlorohexidine
Other Names:
  • Chlorohexidine

What is the study measuring?

Primary Outcome Measures

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

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

May 23, 2024

Primary Completion (Estimated)

May 30, 2024

Study Completion (Estimated)

June 1, 2024

Study Registration Dates

First Submitted

May 14, 2024

First Submitted That Met QC Criteria

May 18, 2024

First Posted (Actual)

May 23, 2024

Study Record Updates

Last Update Posted (Actual)

May 23, 2024

Last Update Submitted That Met QC Criteria

May 18, 2024

Last Verified

May 1, 2024

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • CHX 2024

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Irreversible Pulpitis

Clinical Trials on Irrigating solution

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