Status:
UNKNOWN
3D Instrumentation Versus Rotary Instrumentation
Lead Sponsor:
Cairo University
Conditions:
Postoperative Pain
Eligibility:
All Genders
20-45 years
Phase:
NA
Brief Summary
enrollment of the patient after diagnosis, radiographic evaluation, and signing the informed consent. allocation of the patient to either intervention or control group. After anaesthesia and access c...
Detailed Description
After diagnosing the case as asymptomatic pulp necrosis and confirming that the patient conforms to all eligibility criteria, (R.S) will enroll the patient in the study. the operator will complete tr...
Eligibility Criteria
Inclusion
- Inclusion Criteria:
- Healthy Adult patients.
- Age between 20-40 years old.
- Males \& Females.
- Asymptomatic necrotic mandibular premolars with or without periapical radiolucency.
- Normal occlusal contact with the opposing teeth.
- Patients accepting to participate in the study.
- Exclusion criteria:
- Medically compromised patients
- Pregnant women
- If analgesics or antibiotics have been administrated by the patient during the past 12 hours preoperatively
- Patients reporting bruxism or clenching
- Teeth that shows:
- Association with acute periapical abscess and swelling
- Greater than grade I mobility or pocket depth greater than 5mm
- No restorability
Exclusion
Key Trial Info
Start Date :
November 1 2017
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
November 1 2018
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT03285334
Start Date
November 1 2017
End Date
November 1 2018
Last Update
September 18 2017
Active Locations (1)
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1
Faculty of Oral and Dental Medicine - Cairo University
Cairo, Manial, Egypt, 11553