Evaluation of Corrective Surgery Versus Dental Implants in Compromised Mandibular Molars

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21-60
SponsorAin Shams University

About this trial

This study seeks to assess the clinical, radiographic, and patient-reported outcomes of hemisection versus implant over a 12 months period, generating robust evidence to guide clinical decision-making and enhance patient care.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Good oral hygiene and motivation for follow-up care.

Ability to understand and sign informed consent.

Localized Root/Periodontal Disease: Severe attachment loss or bone loss (e.g., severe localized periodontitis) affecting the mesial root, while the other root remains healthy.

Furcation Involvement: Class II or III furcation involvements where the disease cannot be treated by conventional methods.

Disqualifiers

Uncontrolled systemic diseases (e.g., diabetes mellitus, bleeding disorders, immunosuppression).

Fused or poorly shaped roots,

Active periodontal or endodontic infection at adjacent teeth that may interfere with treatment outcomes.

Severe bruxism or occlusal parafunction.

Trial design

Design model

Parallel

Treatments tested in this trial

  • hemi sectioning

    Procedure/Surgery

    one root will be extracted and the other root will be preserved

Treatment groups

28 Participants
are divided into 2 treatment groups
Group A: HemisectionExperimental treatment 1 intervention
Group B: dental implantsNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

• Regulation of clinical signs and symptoms

Patient-reported outcomes, including satisfaction, masticatory efficiency, and oral comfort measured by a visual analog scale (VAS).

Time frame
12 months

Secondary outcomes

1

Assessment of radiographic bone changes

* Radiographic bone level changes around the retained root or implant. * Detection of any radiographic signs of pathology or treatment failure. Measurements will be recorded in millimeters (mm) using digital radiographic software calibration tools.

Time frame
12 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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