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A clinical study comparing Hemolasertherapy and I-PRF for the treatment of Black triangle

Not Applicable
Conditions
Health Condition 1: K056- Periodontal disease, unspecified
Registration Number
CTRI/2024/08/072144
Lead Sponsor
Deepikashree K
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Subjects exhibiting a healthy periodontium aside from deficient papilla as determined by score 2 of Cardaropoli Papilla Presence Index

Presence of good oral hygiene maintenance

Systemically healthy patients

Non smoker

Exclusion Criteria

Immunocompromised patients

Pregnant and lactating women

Patients who have undergone periodontal surgery in same area within last 6 months

Patients under any medication known to affect the periodontium

Patients with bruxism

Patients exhibiting parafunctional habits and traumatic occlusion

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Papillary RegenerationTimepoint: 1 month 3 months and 6 months
Secondary Outcome Measures
NameTimeMethod
The secondary outcomes will be an improvement in <br/ ><br>Plaque Index <br/ ><br>Gingival Index <br/ ><br>Gingival thicknessTimepoint: 12 TO 18 MONTHS
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