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Not yet recruiting NCT07608497

Evaluation of Corrective Surgery Versus Dental Implants in Compromised Upper Molars

No phase Interventional Root Caries

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: root amputation.
Who it may be relevant to
Registry conditions: Root Caries. Basic parameters: 21 years — 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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

Detailed description

This trial aims to compare periodontal stability, functional outcomes, complications, and patient-reported satisfaction of root amputation versus extraction followed by implant-supported single-tooth restoration. Twenty- eight patients (14 per arm) aged 20-50 with Maxillary first or second molars exhibiting Grade II-III furcation, adequate adjacent bone, and good oral hygiene will be enrolled; exclusions include uncontrolled systemic disease, heavy smoking. Participants will be randomized 1:1 Group A will receive endodontic therapy as indicated, surgical root amputation, while Group B will undergo extraction, and implant placement per standard protocols, and implant crowns. The primary outcome is survival at 12 months; secondary outcomes , clinical attachment level, radiographic bone level, peri-implant/peri-root and prosthetic complications, masticatory function, with clinical and standardized radiographic assessments at 1,3, 6 and 12 months. Data will be statistically analyzed using appropriate tests with significance set at p ≤ 0.05.

Interventions

  • Procedure root amputation
    only one root will be amputated and the rest of the molar will be preserved

Primary outcome measures

  • regression of clinical signs and symptoms and improvement in the bone radiographically [Time frame: 12 months]

Eligibility criteria

Inclusion criteria

  • Patients will be illegible for root amputation if they one or more of the following criteria:
  • Severe vertical bone loss affecting only Mesio-buccal root of Maxillary molar.
  • Through-and-through furcation involvement
  • Vertical root fracture confined to a Mesio-buccal root of Maxillary molar.
  • Extensive root caries affecting Mesio-buccal root of Maxillary molar.
  • Endodontic failure or non- treatable perforation in Mesio-buccal root of Maxillary molar
  • Extensive internal or external non- treatable root resorption related to Mesio-buccal root of Maxillary molar.
  • Patients who do not meet the above criteria and present with Maxillary molars in more severely compromised conditions will be directed for extraction followed by dental implant placement.

Exclusion criteria

  • \- Uncontrolled systemic disease, immunosuppression, recent bisphosphonate use, head and neck radiotherapy.
  • Patient non-compliance or poor oral hygiene.
  • Heavy smoking or inability to commit to maintenance.
  • Root anatomy or interradicular bone that precludes predictable root amputation; insufficient bone for implant placement that cannot be reasonably augmented.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07608497 · 2072021

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗