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Post Operative Pain and Oral Health Related Quality of Life Following Pulpotomy VS Extraction of Permanent First Molar
Sponsor: Cairo University
Summary
The goal of this clinical trial is to compare between post operative pain and oral health related quality of life in participants receiving two treatments for first permanent mandibular molars with poor prognosis. Group I (Experimental group): Complete Pulpotomy with the use of MTA followed by stainless steel crown. Group II (Control group): Non-surgical extraction.
Official title: Post Operative Pain and Oral Health Related Quality of Life Following Pulpotomy VS Extraction for the Management of Permanent First Molar With Poor Prognosis: A Randomized Clinical Trial
Key Details
Gender
All
Age Range
8 Years - 10 Years
Study Type
INTERVENTIONAL
Enrollment
42
Start Date
2024-11
Completion Date
2025-12
Last Updated
2024-05-20
Healthy Volunteers
Yes
Conditions
Interventions
MTA pulpotomy
1. Application of rubber dam for isolation, then a standardized access cavity procedure will be performed using a large sterile round end bur in a high-speed handpiece with copious irrigation, a sharp spoon excavator will remove pulpal tissues to the orifice level, bleeding control in the pulp chamber will be achieved by using 5% sodium hypochlorite. 2. gentle condensation of MTA mix in the pulp chamber will be done by a wet sterile cotton pellet and then the rest of the pulp chamber will be filled with Glass Ionomer restoration. 3. The tooth will be restored with a stainless steel crown.
Extraction
After complete Anesthetic application in the affected area, non-surgical extraction will be done.
Locations (1)
Cairo University
Cairo, Egypt