Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07633834

Evaluation of Corrective Surgery Versus Dental Implants in Compromised Mandibular Molars

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.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

21 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.
  • Vertical root fracture confined to the mesial root.
  • Non-treatable perforation in the mesial root.
  • Extensive sub-gingival root caries affecting the mesial root.
  • Extensive un-treatable internal and external root resorption related to the mesial root.

Exclusion criteria

  • 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.
  • History of radiation therapy in the head and neck region.
  • Pregnancy or lactation.
  • Poor compliance or inability to attend follow-up visits.
  • Smoking more than 10 cigarettes per day.

Treatment and study plan

hemi sectioning

Procedure

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

Primary outcomes

  1. • Regulation of clinical signs and symptoms

    Time frame: 12 months

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

Secondary outcomes

  1. Assessment of radiographic bone changes

    Time frame: 12 months

    • 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.

Sponsors and collaborators

Lead sponsor

Ain Shams University

Other

Registry information

Official study title

Clinical and Radiographic Outcomes of Corrective Surgery Versus Dental Implant Treatment for Management of Compromised Permanent Mandibular Molars (An In-vivo Study)

Important dates

Study start
2027
Primary completion
2027
Study completion
2028
First posted
Jun 8, 2026
Registry last updated
Jun 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.