Clinical Trials Directory

Trials / Completed

CompletedNCT06194721

The Effect of Intra-pulpal Anesthesia With Cryotherapy on Intra-operative Pain

The Effect of Intra-pulpal Anesthesia With Cryotherapy on Intra-operative Pain During Root Canal Treatment on Mandibular Molars With Symptomatic Irreversible Pulpitis

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Gulf Medical University · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Accepted

Summary

The goal of this clinical trial is to compare the effect of cooling of local anesthesia on intraoperative pain during root canal treatment in mandibular molars diagnosed as symptomatic irreversible pulpitis. The main question it aims to answer is: Is there a difference in intra-operative pain levels using intra-pulpal anesthesia with and without cryotherapy during root canal treatment? Participants will undergo root canal treatment using intrapulpal anesthesia with and without cooling. Researchers will compare cold and room temperature intrapulpal anesthesia to see the intensity of intraoperative pain.

Detailed description

The study will be conducted on 40 mandibular molars in each group n = 20. The patient will be asked to pick an opaque sealed envelope that will contain a number 1 or 2. The resultant number will determine in which group the participants will be placed. Double blinding will be maintained in this study as the assessor and the patients will not be aware of their group. Group 1: Will receive intrapulpal local anesthesia at 4-5 C after pulp exposure. Group 2: Will receive intrapulpal local anesthesia at room temperature after pulp exposure. Procedural steps: 1. A history of present illness will be recorded from the patient and the suspected tooth will be tested for vitality using a cold test and an electric pulp tester, to ensure the correct diagnosis is reached. 2. Once the diagnosis is confirmed to be symptomatic irreversible pulpitis, the patient will receive an inferior alveolar nerve block (2% lidocaine 1:100,000). 3. A rubber dam will be used to achieve isolation, and an access cavity will be prepared using a high-speed handpiece, a round bur (no.4), and an Endo-Z bur. 4. If the patient reports feeling any pain, the procedure will stop, and the patient will be presented with a Visual Analogue Scale and asked to rate the pain on a scale of 1-10. Pain levels of more than 5 will be included in the study. 5. Intra-pulpal anesthesia (2% lidocaine 1:100,000) will be administered, and the needle will be surrounded by a piece of sterile gauze to ensure it is under back pressure. 6. After administering the intra-pulpal injection, the patient will again be presented with the same VAS and asked to rate their current pain.

Conditions

Interventions

TypeNameDescription
PROCEDURECold intrapulpal anesthesiaIntrapulpal cold local anesthesia at 4-5 c temperature
PROCEDURERoom temperature intrapulpal anesthesiaIntrapulpal cold local anesthesia at room temperature

Timeline

Start date
2023-06-06
Primary completion
2024-12-06
Completion
2025-01-06
First posted
2024-01-08
Last updated
2025-03-18

Locations

1 site across 1 country: United Arab Emirates

Source: ClinicalTrials.gov record NCT06194721. Inclusion in this directory is not an endorsement.