ROLE OF PRF IN DARKGUMS TREATING WITH TWO SURGICAL METHODS.

Not yet recruiting

Conditions: Other specified disorders of teethand supporting structures,

Registration Number: CTRI/2021/10/037335

Lead Sponsor: PEDDIREDDY TEJASWI

Brief Summary: SOURCE OF DATA:

All the patients will be selected from outpatient Department of Periodontics, Kamineni Institute of Dental Sciences, Narketpally, Nalgonda.

INCLUSION CRITERIA:

1.Age group between 15-45 years.

2.Patients with gingival hyperpigmentation.

3.Systemically healthy patients.

EXCLUSION CRITERIA:

1.Systemically compromised patients and those on medications that may interfere with wound healing.

2.Pregnant women and lactating mother.

3.Patients with a history of severe acute or chronic systemic disease affecting periodontal condition.

4.Patients taking antibiotics for any chronic inflammatory condition

5.Smokers and

6.Endocrine diseases such as addisonâ€™s disease, acromegaly and

Albright`s syndrome7.

SAMPLE SIZE :The study consists of 40 sites which will assigned into four groups.

Group I: 10 Sites- scalpel+ PRF.

Group II: 10 sites- scalpel.

Group III:10 sites- soft tissue trimming bur + PRF.

Group IV: 10 sites- soft tissue trimming bur.

The parameters that will be assessed are:

At baseline:

1.Dummett oral pigmentation Index

2.Epithelization test.

After one week:

1.Visual analog scale [VAS].

2.Healing Index [HI] according to Landry et al.

3.Dummet oral pigmentation Index.

4.Epithelization test.

After 30th day/ 3rd month:

1.Dummet oral pigmentation Index.

Aim :- to evaluate the effectiveness of PRF in wound healing

to compare and evaluate the effect of PRF placed after the treatment of gingival hyperpigmentation with scalpel and soft tissue trimming bur

Detailed Description: Not available

Recruitment & Eligibility

Status: Not Yet Recruiting

Sex: All

Target Recruitment: 40

Inclusion Criteria

Age group between 15-45 years.
GENDER: MALE AND FEMALE Patients with gingival hyperpigmentation.
Systemically healthy patients.

Exclusion Criteria

SMOKERS PREGNANT AND LACTATING WOMENS SYSTEMICALLY COMPROMISED PATIENTS PATIENTS ON ANTIBIOTIC MEDICATIONS.

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Dummett oral pigmentation Index	Base line, fifth day, seventh day, 1 month,3months and months
Epithelization test	Base line, fifth day, seventh day, 1 month,3months and months

Secondary Outcome Measures

Name	Time	Method
Visual analog scale [VAS].	Healing Index [HI] according to Landry et al.

Trial Locations

Locations (1): Kamineni Institute of Dental Sciences
🇮🇳
Nalgonda, TELANGANA, India
Kamineni Institute of Dental Sciences
🇮🇳Nalgonda, TELANGANA, India
Peddireddy Tejaswi
Principal investigator
09491768820
peddireddy.tejaswi@gmail.com