A clinical trial to study the effect of palatal root length on the success of maxillary buccal infiltration by open and closed mouth technique.
Phase 4
Completed
- Conditions
- Health Condition 1: K040- Pulpitis
- Registration Number
- CTRI/2023/01/049312
- Lead Sponsor
- Dr Yogesh K M
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1)Patients aged 18 to 50 years with symptomatic
irreversible pulpitis in maxillary molars.
2)Teeth without gingival recession or existing
periodontal disease.
3)Patients without chronic systemic disease.
4)Patients able to understand pain scales.
Exclusion Criteria
1)Teeth with peri-apical pathology, abscess, sinus
and swelling (non- vital teeth)
2)Teeth with resorptions, calcified canals or
aberrant anatomy.
3)Patients with systemic, immune compromised
disorders including pregnant women.
4)Patients with pace makers.
5)Patients with use of analgesics or anti-
inflammatory drugs 12 hours prior to the
procedure.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method