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PAIN REDUCTION AFTER USING LASER

Phase 4
Conditions
Health Condition 1: K041- Necrosis of pulp
Registration Number
CTRI/2022/11/047168
Lead Sponsor
Dr Rishabhkumar Jain
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Subjects having a single rooted non-vital tooth with closed apex and symptomatic apical periodontitis needing primary endodontic treatment.

Exclusion Criteria

-Subjects with uncontrolled systemic diseases or allergies.

-History of previous root canal treatment.

-Presence of swelling or sinus tracts.

-Presence of severe periodontal disease.

-Subjects whoâ??ve taken analgesics within the last 3 days.

-Subjects allergic to local anesthesia.

-Subjects unwilling to sign the consent form.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
POST OPERATIVE PAINTimepoint: 6,12,24,48 HOURS
Secondary Outcome Measures
NameTimeMethod
ANALGESIC INTAKETimepoint: 6,12,24,48 HOURS
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