Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
ID06698718

Application of CIELab Spectrophotometry to Analyze Gingival Color: a New Perspective for Evaluating the Effectiveness of Periodontal Basic Treatment

Led by Second Affiliated Hospital, School of Medicine, Zhejiang University · Updated on 2024-11-21

30

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the relationship between gum color and clinical signs and inflammatory markers in people with periodontitis. The study plans to include 30 patients diagnosed with periodontitis who visit a hospital's periodontology department between October and November 2024. The goal is to better understand how gum color correlates with inflammation and disease progression. Participants will receive standard periodontal basic treatment. Their age, gender, ethnicity, skin color, and gum type will be recorded. Before treatment and at 6 and 12 weeks afterward, blood tests will measure routine blood counts, high-sensitivity C-reactive protein, and interleukin-6. Samples of gingival fluid will be collected using absorbent paper to assess levels of interleukin-17 and tumor necrosis factor alpha. Clinical measurements including gum color indicators (CIE L*, a*, b*), probing depth, bleeding index, and attachment loss will be recorded before treatment and at 2, 6, and 12 weeks after treatment. Participants will undergo multiple assessments across the study period, including blood tests, gum fluid collection, and clinical exams to track changes in gum color and inflammation. The main outcome measured is the change in gum color values 12 weeks after treatment. The study will analyze and compare data before and after treatment to evaluate the effects of periodontal basic therapy. Participation spans about 12 weeks with several follow-up visits to monitor progress and collect samples.

CONDITIONS

Brief Title

Application of CIELab Spectrophotometry to Analyze Gingival Color: a New Perspective for Evaluating the Effectiveness of Periodontal Basic Treatment

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients of Han ethnicity, aged between 18 and 65 years old, diagnosed with periodontitis
  • No periodontal basic treatment, including scaling, scraping, or flap surgery, in the past six months
  • No periodontal surgery or coronal restoration in the anterior teeth area within six months
  • Clear thinking, able to communicate well, and high compliance
Not Eligible

You will not qualify if you...

  • Cardiac function levels III and IV
  • Blood pressure higher than 180/110 mmHg
  • Pregnant women, women who are pregnant or breastfeeding
  • Taking anticoagulants, calcium channel blockers, immunosuppressants, angiotensin drugs, bisphosphonates treatment, or antibiotics within the last 3 months
  • Uncontrolled or unstable systemic diseases such as progressive liver disease, infectious diseases, kidney failure, rheumatoid disease, blood disorders, osteoporosis, AIDS, mental illness, or diabetes
  • Malignant tumors or undergoing radiotherapy, chemotherapy, or targeted therapy
  • Patients with pacemakers who cannot undergo ultrasound therapy
  • Current smokers or those who quit less than 5 years ago
  • Abnormalities like pigment deposits or keratinized beads on the front teeth or gums

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Single treatment session

Participants receive periodontal basic treatment to manage periodontitis.

1 visit (in-person)

Diagnostic Evaluation

Duration - 12 weeks after treatment

Participants undergo CIELab spectrophotometry to analyze gingival color and evaluate treatment effectiveness.

1 follow-up visit

Trial Site Locations

Total: 1 location

1

2 nd Affiliated Hospital, School of Medicine, Zhejiang University, China

Hangzhou, Zhejiang, China

Actively Recruiting

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Research Team

S

Sun

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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