Last updated: February 6, 2024
Sponsor: Ain Shams University
Overall Status: Completed
Phase
N/A
Condition
N/ATreatment
Dexamethasone sodium phosphate
Cryotherapy
Diclofenac sodium
Clinical Study ID
NCT06090500
FDASU 1234
Ages 18-50 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Egyptian healthy both gender patients (Category: American Society of AnesthesiologistsASA class I)
- Patients age (18- 50) years old.
- Maxillary premolar teeth diagnosed with symptomatic irreversible pulpitis.
- No clinical or radiographic evidence of periapical nor periodontal pathosis.
- Compliant patient.
Exclusion
Exclusion Criteria:
- The vulnerable group; prisoners, pregnant females, mentally ill, severe systemicdiseases, psychological diseases, TMJ problems.
- Analgesics or anti-inflammatory drugs taken within 24 h before the intervention.
- Over instrumentation during treatment.
- Long-term use of corticosteroids.
- Access revealing necrotic tooth indicating a false positive diagnosis.
- Sensitivity to any of the pharmaceuticals intended to be used in this study.
- Intra operative complications such as canal calcification, or loss of apical Patency.
Study Design
Total Participants: 52
Treatment Group(s): 3
Primary Treatment: Dexamethasone sodium phosphate
Phase:
Study Start date:
March 20, 2023
Estimated Completion Date:
January 30, 2024
Study Description
Connect with a study center
Ain Shams University
Cairo,
EgyptSite Not Available
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.