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A Study Comparing The Functional And Esthetic Outcomes Of Patients Undergoing Corrective Surgery For Old Facial Fractures That Have Healed in the Wrong Position, Using Computer-Based 3D Virtual Surgical Planning Versus Conventional Planning.

NCT07920445, Not applicable, Completed, University of Health Sciences Lahore

Trial 10

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

FieldValueSource
Title
A Study Comparing The Functional And Esthetic Outcomes Of Patients Undergoing Corrective Surgery For Old Facial Fractures That Have Healed in the Wrong Position, Using Computer-Based 3D Virtual Surgical Planning Versus Conventional Planning.
ClinicalTrials.gov
NCT numberNCT07920445ClinicalTrials.gov
StatusCompletedClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment50 participants, actualClinicalTrials.gov
Lead sponsorUniversity of Health Sciences LahoreClinicalTrials.gov
ConditionsFacial Fractures, Maxillofacial Trauma, Malunited Maxilla FractureClinicalTrials.gov
InterventionsPanfacial Fracture Reduction and Fixation, Panfacial Fracture Reduction and Fixation Using Pre-bent Plates Guided by Virtual Surgical PlanningClinicalTrials.gov
First posted2026-11-05ClinicalTrials.gov
Last updated2026-11-05ClinicalTrials.gov

Registered outcomes 6

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

ListOutcomeTime frameDescriptionSource
PrimaryMalocclusionFrom enrollment to the end of treatment at 12 weeks
Deviation from normal occlusion in which teeth are not in their normal relation to the adjacent teeth in the same jaw and to the opposing teeth when the jaw is closed. Post traumatic malocclusion includes anterior open bite, posterior open bite, anterior cross bite, posterior cross bite and, gagging of occlusion. Malocclusion was assessed on clinical examination
ClinicalTrials.gov
SecondaryOperation timeDuring intervention(surgery)The time from marking the first incision till placement of final dressing after closure.ClinicalTrials.gov
SecondaryEnophthalmosFrom enrollment to the end of treatment at 12 weeks
Characterized as backward displacement of eyeball. It will be measured on axial slice of CT scan face. A line connecting bilateral anterior tips of lateral walls will be made. After identifying center of cornea, a vertical line perpendicular to first line will be drawn bilaterally. Difference of both perpendicular lines is enophthalmos measurement. Every cm3 increase in volume is represented by approximately 0.77mm.
ClinicalTrials.gov
SecondaryAnthropometric facial measurementsFrom enrollment to the end of treatment at 12 weeks
Anthropometry is 'study of measurements of human body' and Anthropometric facial measurements are 'linear distances which are measured using anatomical landmarks at predefined locations on face'. It includes Upper facial height ,Middle facial height, Lower facial height, Maximal facial breadth and Bigonal breadth.
ClinicalTrials.gov
SecondaryQuality of life questionnaireAfter intervention till the end of treatment at 12 weeks
A set of survey questions that can be used to collect data related to an individual in particular to determine their general quality of life, health, living condition and more.Questionnaire is based on a validated Dutch questionnaire and it includes questions about isolation from work, social isolation, ability to eat, ability to speak, influence on sleep, facial appearance, and satisfaction with the given treatment
ClinicalTrials.gov
SecondaryNumber of readjustments of prebent platesDuring Intervention (surgery)Peroperative rebending of already bent plate in patients receiving preoperative virtual surgical planningClinicalTrials.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 2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
18022469BACKGROUNDPubMed
31345490BACKGROUNDPubMed

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)