Trial · NCT07904897
Optimized Osteosynthesis: Bone Mineral Density Recovery in Mandibular Body Fractures Using Patient-Specific Versus Conventional Plates
NCT07904897, Not applicable, Recruiting, Cairo University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Optimized Osteosynthesis: Bone Mineral Density Recovery in Mandibular Body Fractures Using Patient-Specific Versus Conventional Plates. Trials, record NCT07904897. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07904897
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Optimized Osteosynthesis: Bone Mineral Density Recovery in Mandibular Body Fractures Using Patient-Specific Versus Conventional Plates
- NCT number
- NCT07904897
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 26 participants, estimated
- Lead sponsor
- Cairo University
- Conditions
- Mandibular Fractures
- Interventions
- Open reduction and Internal fixation of a mandibular body fracture, Open reduction and Internal fixation of a mandibular body fracture
- First posted
- 2026-10-29
- Last updated
- 2026-10-29
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Bone density | Patients will undergo multi-slice CT scanning at baseline (within 1 week) and at 6 months postoperatively to assess the recovery. | Bone mineral density recovery at the fracture site, will be analyzed using Hounsfield Units (HU). |
| Secondary | Postoperative occlusion | One week postoperatively | Number of participants achieving a satisfactory occlusion, defined as meeting three criteria simultaneously: dental midline deviation ≤ 1 mm, bilateral normal canine relationship, and bilateral normal molar relationship. Failure in any criterion is classified as unsatisfactory. |
| Secondary | Incidence of Postoperative Neurosensory Dysfunction | One week postoperatively | The number of participants who develop neurosensory dysfunction. Sensation is evaluated using the Two-Point Discrimination (2PD) test. Neurosensory dysfunction is defined as a binary categorical outcome where a participant fails to distinguish two distinct points at the standard clinical threshold (≤ 5 mm). Participants who require a distance greater than 5 mm to discriminate the two points are marked as having neurosensory dysfunction. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers13
The papers the trial lists on ClinicalTrials.gov.
Grants0
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.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07904897
GET https://conductscience.org/api/trials/v1/NCT07904897/registered