A study for comparing the efficiency of two techniques , using injectable platelet rich fibrin and connective tissue grafting in gum reconstructio

Phase 3

• Conditions: Health Condition 1: K060- Gingival recession

• Registration Number: CTRI/2024/05/067043
• Lead Sponsor: Dr Jeswin Johnson

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 27 May 2024

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1. Otherwise systematically healthy individuals having at least one Nordland and Tarnows

Class I or Class II open gingival or cervical embrasure in maxillary anterior region

2. FMBS and FMPS less than 20 percentage

3. Selected teeth must be free of restorations on the cervical (buccal or proximal) region

4. Radiographically, the distance between contact point (CP) to alveolar crest should be less than or equal to 6 mm

5. Minimal probing depth (less than or equal to 2 mm) adjacent to the open embrasure

Exclusion Criteria

1. Smokers

2. Pregnant or lactating women

3. Previous periodontal surgery.

4. Undergoing active orthodontic treatment

5. Tooth mobility bruxism, missing or supernumerary teeth, mucogingival problem

(shallow vestibule, aberrant frenemy attachment, or inadequate zone of attached

gingiva)

6) Patients allergic to Ibuprofen

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Change in interdental papilla height .Timepoint: baseline (0) <br/ ><br>After 1 month <br/ ><br>After 3 months

Secondary Outcome Measures

Name	Time	Method
Change in black triangle <br/ ><br>height <br/ ><br>Probing pocket depth (PPD) change <br/ ><br>Clinical attachment level <br/ ><br>(CAL) gain <br/ ><br>Timepoint: baseline (0) <br/ ><br>After 1 month <br/ ><br>After 3 months