Pain Clinical Trial
Official title:
Comparison of the Efficacy of Calcium Hydroxide Combined With Silver Nano Particulate and Conventional Calcium Hydroxide Intra Canal Medications on Post-Operative Pain in Symptomatic Root Canal Treatment Failure Cases: A Randomized Clinical Trial Therapeutic Study
The aim of this study is to measure and compare the effectiveness of nanosilver combined calcium hydroxide and conventional calcium hydroxide intracanal medications in reducing postoperative pain in patients with Symptomatic Root Canal treatment Failure .
- After confirming the diagnosis and making sure that the patient conforms to all
eligibility criteria, the principal investigator will enroll the patient in the study.
- The operator will complete treatment of all cases in two visits as follows:
1. First session:
- Patients will be asked to rate their pain level on NRS before treatment is
started.
- Patient will be anesthetized by using nerve block local anesthesia or
infiltration local anesthesia according to the tooth location in mandibular or
maxillary arch respectively.
- Previous coronal restoration will be removed:
- If the access will be cut through metal (amalgam alloy or cast metal) or
composite resin, carbide fissure bur will be used.
- In case of porcelain fused to metal (PFM) crown a round diamond is used
to cut through the porcelain layer, then Transmetal bur is used to cut
through and remove the core material.
- Teeth will be isolated with rubber dam.
- Gutta percha removal will be done using protaper rotary retreatment files in
the following manner D1 has a cutting tip to facilitate initial penetration
into the filling material (coronal third). D2 and D3 both have non-cutting
tips and are used to remove material from the middle and apical thirds,
respectively using gutta percha solvent
- Working length will be determined using an electronic apex locator then
confirmed with intraoral periapical radiograph, to be 0.5-1 mm, shorter than
radiographic apex.
- Cleaning and shaping will be done using crown down preparation technique with
the use of protaper rotary files in an endodontic motor according to the
manufacturer instructions, the canals will be thoroughly irrigated using 3ml
of 2.5% Sodium hypochlorite between every subsequent instruments.
- MD-Chelcream will be used as lubricant during mechanical preparation.
- After instrumentation of the canals paper points (Protaper Paper Points) will
be used for drying.
- Using Lentulo Spiral Filler, medicaments will be placed under aseptic
conditions into the canals according to each group, Experimental group Ca (OH)
2 ( Ca (OH) 2with nanosilver suspension and comparison group Ca (OH) 2 with
sterile water then access cavity will be closed with a temporary filling
- Patient will be instructed to call in case of severe pain in between visits,
an emergency analgesics are to be prescribed to the patient (Brufen 400mg)
2. Second session:
- After 7 days, rubber dam will be placed , the temporary fillings will be
removed and master apical file will be introduced in each root canal to loosen
medicament and to create a space for subsequent irrigant, then each root canal
will be washed with 5 mL of sterile saline, irrigated with 1 mL of 20% citric
acid and again irrigated with 5 mL sterile saline.
- Dryness of the canals by paper points (Protaper Paper Points).
- Obturation will be carried out using the cold lateral condensation technique
with protaper gutta percha cones and resin sealer with spreader size according
to master cone size , its depth short 2 mm of the working length, and
auxiliary cones size 25.
- After obturation a cotton pellet will be placed in the pulp chamber and the
access cavity will be closed with a temporary filling to avoid coronal
leakage.
- The patient is given a NRS and asked to rate his pain level at 6, 12, 24 & 48
hours after root canal retreatment .
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT05559255 -
Changes in Pain, Spasticity, and Quality of Life After Use of Counterstrain Treatment in Individuals With SCI
|
N/A | |
Completed |
NCT04748367 -
Leveraging on Immersive Virtual Reality to Reduce Pain and Anxiety in Children During Immunization in Primary Care
|
N/A | |
Terminated |
NCT04356352 -
Lidocaine, Esmolol, or Placebo to Relieve IV Propofol Pain
|
Phase 2/Phase 3 | |
Completed |
NCT05057988 -
Virtual Empowered Relief for Chronic Pain
|
N/A | |
Completed |
NCT04466111 -
Observational, Post Market Study in Treating Chronic Upper Extremity Limb Pain
|
||
Recruiting |
NCT06206252 -
Can Medical Cannabis Affect Opioid Use?
|
||
Completed |
NCT05868122 -
A Study to Evaluate a Fixed Combination of Acetaminophen/Naproxen Sodium in Acute Postoperative Pain Following Bunionectomy
|
Phase 3 | |
Active, not recruiting |
NCT05006976 -
A Naturalistic Trial of Nudging Clinicians in the Norwegian Sickness Absence Clinic. The NSAC Nudge Study
|
N/A | |
Completed |
NCT03273114 -
Cognitive Functional Therapy (CFT) Compared With Core Training Exercise and Manual Therapy (CORE-MT) in Patients With Chronic Low Back Pain
|
N/A | |
Enrolling by invitation |
NCT06087432 -
Is PNF Application Effective on Temporomandibular Dysfunction
|
N/A | |
Completed |
NCT05508594 -
Efficacy and Pharmacokinetic-Pharmacodynamic Relationship of Intranasally Administered Sufentanil, Ketamine, and CT001
|
Phase 2/Phase 3 | |
Recruiting |
NCT03646955 -
Partial Breast Versus no Irradiation for Women With Early Breast Cancer
|
N/A | |
Active, not recruiting |
NCT03472300 -
Prevalence of Self-disclosed Knee Trouble and Use of Treatments Among Elderly Individuals
|
||
Completed |
NCT03678168 -
A Comparison Between Conventional Throat Packs and Pharyngeal Placement of Tampons in Rhinology Surgeries
|
N/A | |
Completed |
NCT03931772 -
Online Automated Self-Hypnosis Program
|
N/A | |
Completed |
NCT03286543 -
Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty Using the SPRINT Beta System
|
N/A | |
Completed |
NCT02913027 -
Can We Improve the Comfort of Pelvic Exams?
|
N/A | |
Terminated |
NCT02181387 -
Acetaminophen Use in Labor - Does Use of Acetaminophen Reduce Neuraxial Analgesic Drug Requirement During Labor?
|
Phase 4 | |
Recruiting |
NCT06032559 -
Implementation and Effectiveness of Mindfulness Oriented Recovery Enhancement as an Adjunct to Methadone Treatment
|
Phase 3 | |
Active, not recruiting |
NCT03613155 -
Assessment of Anxiety in Patients Treated by SMUR Toulouse and Receiving MEOPA as Part of Their Care
|