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Efficacy of Submucosal Tramadol and Lidocaine on Success Rate of Inferior Alveolar Nerve Block in Mandibular Molars with Symptomatic Irreversible Pulpitis

Not Applicable
Completed
Conditions
patients with symptomatic irreversible pulpitis
Irreversible pulpitis
mandibular molar
lidocaine
supplemental anesthesia
submucosal injection
tramadol
Registration Number
TCTR20190509004
Lead Sponsor
none
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
105
Inclusion Criteria

1. A single mandibular molar tooth responding to cold test for a long time and diagnosed with symptomatic irreversible pulpitis
2. Patients with preoperative pain scores ranging from moderate to severe (55â€170 mm) on a Heft-Parker visual analog scale (HP VAS, 0â€170 mm)
3. The absence of periapical radiolucency on periapical radiography (except enlarged periodontal ligaments not larger than 0.75-1 mm)
4. Have the ability to understand the informed consent form and pain record scales to be used within the study

Exclusion Criteria

1. Receiving analgesic or anti-inflammatory drugs within 24 hours prior to treatment
2. Allergy or susceptibility to any opioid or nonopioid analgesia, including lidocaine, tramadol or NSAIDs
3. Pregnant or nursing, those with any bleeding problem or those using anticoagulant medication
4. Patients have not lip numbness following initial IANB injection
4. In addition to hypersensitive teeth to percussion and palpation; teeth have calcified root canals, periodontal diseases, root resorption, open apex, necrotic pulp and have already been undergone root canal treatment were excluded from the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
pulpal anesthesia 15 minutes HP VAS Scale
Secondary Outcome Measures
NameTimeMethod
preparation pain 15 minutes HP VAS Scale
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