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Clinical Trials/NCT07246174
NCT07246174CompletedNot Applicable

Comparison of AH Plus and WellRootST Root Canal Sealers in Terms of Postoperative Pain: One-Month Follow-up

Medipol University1 site in 1 country120 target enrollmentStarted: January 1, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
120
Locations
1
Primary Endpoint
postoperative pain evaluation by VAS scale

Study Overview

Brief Summary

The objective of this research was to identify which of the root canal sealers, AH Plus or WellRootST, yielded more effective outcomes regarding postoperative pain when applied to teeth diagnosed with apical periodontitis.

Detailed Description

A prospective cohort study was conducted at a single center, involving 120 patients diagnosed with chronic apical periodontitis (AP) admitted for endodontic treatment. Patients were categorized into two groups based on the type of root canal sealer used. Sixty patients treated with AH Plus sealer constituted Group 1, while sixty patients treated with WellRootST sealer comprised Group 2. Data collected for all participants included age, gender, findings from oral and dental examinations, tooth type, tooth number, duration of root canal treatment, and Visual Analog Scale (VAS) results recorded preoperatively, as well as at 24 hours, 48 hours, 72 hours, 1 week, and 1 month postoperatively.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •The inclusion criteria for this study were as follows:
  • •Participants had to be at least 18 years old
  • •One mature tooth showing signs or symptoms that required primary root canal treatment.
  • •Participants needed to be in good general health
  • •classified as ASA I or II, and able to follow the follow-up schedule.

Exclusion Criteria

  • •criteria for this study were as follows:
  • •Included teeth with internal or external root resorption,
  • •Signs of perforation
  • •The need for post-core application, or previous restoration with fixed prosthetic appliances, such as crowns or bridges

Arms & Interventions

AhPlus sealer

Experimental

AH Plus sealer used

Intervention: AH-Plus Epoxy Resin Sealer (Procedure)

WellRootST sealer

Experimental

WellRootST sealer used

Intervention: bioceramic sealer (Procedure)

Outcomes

Primary Outcomes

postoperative pain evaluation by VAS scale

Time Frame: Baseline, 24 hour postoperatively, 48hour postoperatively, 72 hour postoperatively, Day 3 and Day 7

Study groups were compared in terms of VAS scores at the preoperative period and postoperative 24 hours, 48 hours, 72 hours, 1 week, and 1 month

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Medipol University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Furkan Salih Bilgi

Principal Investigator

Medipol University

Study Sites (1)

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