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Not yet recruiting NCT06804330

Evaluation of Postoperative Pain and Antimicrobial Efficacy of Selenium Versus Calcium Hydroxide As Intracanal Medication in Mandibular First Molars with Necrotic Pulp and Symptomatic Apical Periodontitis

No phase Interventional Necrotic Pulp with Symptomatic Apical Periodontitis Postoperative Dental Pain Antimicrobial Effect

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: root canal treatment and intracanal medicament.
Who it may be relevant to
Registry conditions: Necrotic Pulp with Symptomatic Apical Periodontitis, Postoperative Dental Pain, Antimicrobial Effect. Basic parameters: 20 years — 40 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The main rational behind intracanal medicament is to kill the bacteria inside the root canal and to avert reinfection. In absence of nutrients, the bacteria remains after obturation in root canal may not survive. Otherwise they may flourish \& If the root canal is not dressed properly with antiseptic medicaments between the visits, the residual bacteria may increase . Thus the use of effective intracanal medication for disinfection of root canal is necessitated . Medicament with long effect and least irritated to periradicular tissue has to be introduced to infiltrate the dentinal tubule eliminating bacteria . As the effect of intracanal medicaments is longer than irrigants, it is generally recommended to fill the root canal between appointments with intracanal medicaments. Calcium hydroxide is the most commonly recommended antimicrobial agent for interappointment medications. It serves as an effective intracanal medicament due to its alkaline pH, which inhibits bacterial growth. However, calcium hydroxide has limitations. .Recently selenium(Se) was introduced as intracanal medication .Se is a mineral essential for the formation of the amino acid selenocysteine, which is directly involved in the maintenance of the immune response. Selenium has been widely used in the medical field in the treatment of cancer, as an activator of bone metabolism, and as a stimulator of the immune system. In this study, it will show that the incorporation of Se, whether as intracanal medication alone or in conjunction with other medications, may potentiate periapical tissue repair after RCS cleaning and shaping procedures. This study consists of 60 patients divided into 3 group each group having 20 patient. Intervention 1: intracanal medication using selenium alone . Intervention 2: intracanal medication using selenium with calcium hydroxide

Interventions

  • Procedure root canal treatment and intracanal medicament
    Root canal biomechanical preparation followed by intracanal placement of intracanal medicament according to the arm

Primary outcome measures

  • Post-operative pain [Time frame: 6 hours up to 96 hours]
Secondary outcome measures (1)
  • Bacterial Load [Time frame: Before intracanal medication injection and 2 weeks following the procedure and before obturating the root canals]

Eligibility criteria

Inclusion criteria

  • Medically free patients with no systemic disease: (American Society of Anesthesiologists / (ASA Class I or II).
  • Age range is between 20 to 40 years.
  • No sex predilection.
  • Patients having necrotic pulp with symptomatic apical periodontitis in mandibular first molars.(type l distal root canal ) .
  • Sensitive to percussion.
  • Periapical radiographic appearance of teeth showed slight widening in lamina dura.
  • restorable teeth.
  • Positive patient"s acceptance for participating in the study.
  • Patients able to sign informed consent.

Exclusion criteria

  • Medically compromised patients.
  • Pregnant or lactating females.
  • Psychologically disturbed patients.
  • Patients with a history of allergy to any medication used in the study were excluded.
  • If anti-inflammatory analgesics or antibiotics have been administrated by patient during the past 12 hours preoperatively.
  • Patients with swelling or acute peri-apical abscess or fistulous tract.

Teeth that have:

  • Wide or open apex.
  • Vital pulp tissues.
  • Periodontally affected with grade 2 or 3 mobility.
  • Not restorable teeth.
  • Abnormal anatomy and calcified canals.
  • Previous root canal treatment.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Triple blind
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06804330 · FUE.REC(15)/6-2024

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗