Ignite Creation Date:
2024-05-06 @ 7:57 PM
Last Modification Date:
2024-10-26 @ 3:18 PM
Study NCT ID:
NCT06207019
Status:
COMPLETED
Last Update Posted:
2024-01-16
First Post:
2024-01-05
Brief Title:
Post-Operative Pain Evaluation After Using Different Single-file Root Canal Preparation System A Randomized Clinical Study
Sponsor:
Tanta University
Organization:
Tanta University
Study Overview
Official Title:
Post-Operative Pain Evaluation After Using Different Single-file Root Canal Preparation System A Randomized Clinical Study
Status:
COMPLETED
Status Verified Date:
2024-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this clinical trial is to assess post-operative pain following root canal preparation using various single-file systems
Detailed Description:
The goal of this clinical trial is to assess post-operative pain following root canal preparation using various single-file systemsPostoperative pain assessment was done by an independent evaluator with no knowledge of the group under investigation The visual Analogue Scale VAS was employed Patients could put a mark anywhere on the VAS sheet with values ranging from 0 to 100 mm 10
Score 0 No pain between 0 and 4 mm the tooth after treatment felt normal and no discomfort was reported by the patients
Score 1 Recognizable mild pain between 5 and 44 mm not requiring analgesics
Score 2 Moderate pain between 45 and 74 mm that is uncomfortable but bearable when analgesics were taken the pain was successfully reduced
Score 3 Severe pain between 75 and 100 mm painful to endure pain was not relieved by taking analgesics
The patients in this study were not aware of the preparation system used during treatment Following treatment three readings were taken at 24 72 and 7 days Each patient carried a VAS form and reminder calls were made to record pain levels and return the form filled out completely
Score 0 No pain between 0 and 4 mm the tooth after treatment felt normal and no discomfort was reported by the patients
Score 1 Recognizable mild pain between 5 and 44 mm not requiring analgesics
Score 2 Moderate pain between 45 and 74 mm that is uncomfortable but bearable when analgesics were taken the pain was successfully reduced
Score 3 Severe pain between 75 and 100 mm painful to endure pain was not relieved by taking analgesics
The patients in this study were not aware of the preparation system used during treatment Following treatment three readings were taken at 24 72 and 7 days Each patient carried a VAS form and reminder calls were made to record pain levels and return the form filled out completely
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None