Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07527351

Analysis of the Reliability and Validity of Laser Speckle Contrast Imaging

Led by Universidad Complutense de Madrid · Updated on 2026-04-22

24

Participants Needed

1

Research Sites

5 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is designed to validate laser speckle contrast imaging (LSCI) as a non-invasive method for measuring superficial gingival blood perfusion. Accurate assessment of vascularization is essential for understanding periodontal and peri-implant wound healing, yet current clinical methods are limited by subjective interpretation and low reproducibility. Repeated LSCI measurements will be performed in healthy gingival tissues and in tissues undergoing different mucogingival healing patterns, including primary and secondary intention healing. The study will also evaluate factors that may influence perfusion readings, such as angulation, retractors, mirror use, temperature, and heart rate. The primary objective is to determine the reproducibility of LSCI measurements and to support its use as a reliable tool for monitoring oral soft-tissue vascularization and healing.

CONDITIONS

Official Title

Analysis of the Reliability and Validity of Laser Speckle Contrast Imaging

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Non-smokers
  • Good systemic health
  • Good periodontal health
  • No current systemic medication
  • Good oral hygiene
  • For the retrospective surgical component: availability of previously documented clinical records from closed mucogingival surgical wounds or open palatal donor-site wounds, with prior consent allowing use of documented clinical material for research
Not Eligible

You will not qualify if you...

  • Pregnancy
  • Use of anti-inflammatory medication within 7 days before evaluation
  • Oral treatment within 6 months before evaluation
  • For the prospective healthy-gingiva component: any condition not compatible with good systemic or periodontal health
  • For the retrospective surgical component: absence of adequate previously documented clinical records or absence of prior consent for research use of the documented material

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Complutense University of Madrid

Madrid, Madrid, Spain, 28040

Actively Recruiting

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Research Team

M

Mariano Sanz Alonso, DMD, MD, PHD

CONTACT

M

Mercedes Lopez Duran, DMD, PHD

CONTACT

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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