Evaluation of Post Operative Pain & Success Rate After Pulpotomy

Status Recruiting

Clinical Trial Summary

The aim of this randomized controlled trial is to assess the post-operative pain as primary outcome and the success rate as secondary outcome after pulpotomy using different calcium silicate based materials in mature permanent teeth diagnosed with irreversible pulpitis.

Clinical Trial Description

Setting and location : Out-patients clinic of Endodontic Department, Faculty of Dentistry, Ain Shams University Patient allocation: Using computer generated randomization (www.randome.org), the participants will allocated randomly into three groups . The sequentially numbers that will be generated, will be placed in opaque envelope until the intervention and each participant will be asked to select an envelope that determine which group of intervention he will be assigned. Patient Classification: Patients will be randomly divided into three groups according to material used in pulpotomy Group (1) Biodentine (n=20) Group (2) theracal PT (n=20) Group (3) Neoputty (n=20) Procedural steps: - Pain scale chart will be given to each patient to rate his /her pain level before endodontic treatment as preoperative reading on a visual analogue scale (VAS) - Tooth will be anaesthetized using Local anesthesia containing Articaine with epinephrine 1:100,000. - Rubber dam isolation of tooth - Tooth surface disinfection using guaze soaked in 5.25% sodium hypochlorite - Access cavity will be performed using a carbide steel round bur and tapered diamond stone until complete deroofing. - Using a sterile excavator, the coronal pulp tissue will be excavated14 - Cotton pellets soaked in 2.5 % sodium hypochlorite will be used to achieve hemostasis for 2-3 minutes - Once hemostasis will be achieved one of the three materials will be placed according to the manufacturer's instructions - Final restoration will be placed Methods of evaluation 1. Post operative pain 2. Pulpotomy success rate ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04933955
Study type	Interventional
Source	Ain Shams University
Contact	Ahmed Abdel Rahman m Hashem, phd
Phone	226401884
Email	ahmed@endohashem.com
Status	Recruiting
Phase	N/A
Start date	June 1, 2021
Completion date	December 1, 2022

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Evaluation of Post Operative Pain and Success Rate After Pulpotomy

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms