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Microneedling-Assisted Hyaluronic Acid for Interdental Papilla Deficiency

NCT07919808, Not applicable, Not yet recruiting, Badr University

Trial 10

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleMicroneedling-Assisted Hyaluronic Acid for Interdental Papilla DeficiencyClinicalTrials.gov
NCT numberNCT07919808ClinicalTrials.gov
StatusNot yet recruitingClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment20 participants, estimatedClinicalTrials.gov
Lead sponsorBadr UniversityClinicalTrials.gov
ConditionsInterdental Papilla DeficiencyClinicalTrials.gov
InterventionsMicroneedling, cross-linked hyaluronic acidClinicalTrials.gov
First posted2026-11-05ClinicalTrials.gov
Last updated2026-11-06ClinicalTrials.gov

Registered outcomes 8

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryChange in Black Triangle HeightBaseline, 1 month, 3 months, and 6 months
Black triangle height will be measured in millimeters as the linear distance from the base of the interproximal contact point to the most coronal tip of the interdental papilla using a calibrated UNC-15 periodontal probe. Standardized acrylic stents will be used to ensure reproducible probe angulation and reference point positioning.
ClinicalTrials.gov
SecondaryGingival Crevicular Fluid Periostin LevelBaseline, 1 month, 3 months, and 6 monthsPeriostin concentration in gingival crevicular fluid will be measured using a commercially available human periostin ELISA kit.ClinicalTrials.gov
SecondaryGingival Crevicular Fluid MMP-9 LevelBaseline, 1 month, 3 months, and 6 monthsMMP-9 concentration in gingival crevicular fluid will be measured using a commercially available human MMP-9 ELISA kit.ClinicalTrials.gov
SecondaryGingival Crevicular Fluid TIMP-1 LevelBaseline, 1 month, 3 months, and 6 monthsTIMP-1 concentration in gingival crevicular fluid will be measured using a commercially available human TIMP-1 ELISA kit.ClinicalTrials.gov
SecondaryPlaque IndexBaseline, 1 month, 3 months, and 6 monthsPlaque accumulation will be assessed using the Silness and Löe Plaque Index on a score from 0 to 3.ClinicalTrials.gov
SecondaryGingival IndexBaseline, 1 month, 3 months, and 6 monthsGingival inflammation will be assessed using the Löe and Silness Gingival Index on a score from 0 to 3.ClinicalTrials.gov
SecondaryPeriodontal Probing DepthBaseline, 1 month, 3 months, and 6 monthsPeriodontal probing depth will be measured in millimeters from the gingival margin to the base of the sulcus or periodontal pocket using a UNC-15 periodontal probe.ClinicalTrials.gov
SecondaryPatient Satisfaction6 monthsPatient satisfaction with esthetic appearance will be assessed using a visual analogue scale at the end of the follow-up period.ClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Grants 0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)