NCT06427070

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.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
1

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2024

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 14, 2024

Completed
9 days until next milestone

First Posted

Study publicly available on registry

May 23, 2024

Completed
Same day until next milestone

Study Start

First participant enrolled

May 23, 2024

Completed
7 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 30, 2024

Completed
2 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2024

Completed
Last Updated

May 23, 2024

Status Verified

May 1, 2024

Enrollment Period

7 days

First QC Date

May 14, 2024

Last Update Submit

May 18, 2024

Conditions

Irreversible Pulpitis

Keywords

PulpitisCHXSaline

Outcome Measures

Primary Outcomes (2)

  • pain scale

    pain scale Comparison of the 2 selected irrigating solutions

    1 week

  • Analgesics Frequency

    Frequency of analgesics for pain relief

    1 week

Study Arms (1)

Irrigating solutions

EXPERIMENTAL

Group 1 sodium hypochlorite Group 2 saline Group 3 chlorohexidine

Other: Irrigating solution

Interventions

Irrigating solutionOTHER

Saline, sodium hypochlorite, chlorohexidine

Also known as: Chlorohexidine
Irrigating solutions

Eligibility Criteria

Age25 Years - 50 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Pulpitis

Interventions

dextran - saline drug combination

Condition Hierarchy (Ancestors)

Dental Pulp DiseasesTooth DiseasesStomatognathic Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer at Misr university

Study Record Dates

First Submitted

May 14, 2024

First Posted

May 23, 2024

Study Start

May 23, 2024

Primary Completion

May 30, 2024

Study Completion

June 1, 2024

Last Updated

May 23, 2024

Record last verified: 2024-05