Status:
NOT_YET_RECRUITING
Evaluation of the Effect of Intra-ligamentary Injection of Diclofenac Potassium Versus Articaine on Anaesthetic Efficacy in Mandibular Molars With Symptomatic Irreversible Pulpitis.
Lead Sponsor:
Cairo University
Conditions:
Teeth With Acute Irreverseble Pulpitis
Eligibility:
All Genders
18-55 years
Phase:
EARLY_PHASE1
Brief Summary
This study aims to assess the effect the intraligamentary injection of Diclofenac Potassium versus Articaine 4% on the anaesthetic efficacy \& intensity of intraoperative \& postoperative pain during ...
Eligibility Criteria
Inclusion
- Systemically healthy patient (ASA I or II).
- Mandibular Posterior teeth with:
- Preoperative sharp pain, Absence or slight widening in the periodontal ligament (PDL), Vital response of pulp tissue to cold pulp test.
- patients who agree to provide written consent and the patients able to understand the pain scale and attend for recall appointments
Exclusion
- Patients allergic to anesthetic solutions \& other NSAIDs.
- Pregnant or nursing females.
- Patients having significant systemic disorder (ASA III or IV).
- Gastrointestinal disorders.
- If the initial diagnosis revealed pain in more than one tooth.
- Hemostatic disorders or anti-coagulant therapy during the last month.
- Consumption of opioid or non-opioid analgesics or NSAIDs during the last 12 hours before treatment.
- Teeth that have:
- i. Periodontal involvement (with pocket depth greater than 5mm, associated with swelling or fistulous tract, or greater than grade I mobility).
- ii. No possible restorability. iii.Signs of pulpal necrosis; associated sinus tract or swelling.
- \-
Key Trial Info
Start Date :
August 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
July 1 2025
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT06500871
Start Date
August 1 2024
End Date
July 1 2025
Last Update
August 6 2024
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