Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06808854

Variable-thread Versus Standard Dental Implants for Replacing Missing Teeth

Led by Mohammed Bin Rashid University of Medicine and Health Sciences · Updated on 2025-07-01

24

Participants Needed

1

Research Sites

117 weeks

Total Duration

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AI-Summary

What this Trial Is About

Background and objectives: Primary and secondary implant stability remain the most relevant and reliable clinical indicator for long-term survival of dental implants. Hence modifications of surface characteristics and implant macro-designs were introduced over the last two decades to enhance osseointegration during the initial phase of healing. In this context, a variable-thread self-cutting implant design was recently introduced to improve primary stability. At present, there are limited number of studies that evaluated this variable-thread implant design. These studies were mostly experimental, of short duration and limited number of participants. Therefore, the aim of the present randomized controlled trial is to compare two implant designs (variable-thread versus standard) in terms of clinical, radiographic and patient-reported outcomes. Methods: A total of 24 participants, who require replacement of a posterior single tooth with dental implant, will be randomly allocated to two equal sized groups. In the test group, the participants will receive variable-thread implants, while standard implants will be placed to replace missing teeth in the control group. In addition to evaluating implant stability, the trial will also report on clinical and radiographic implant outcomes at various time points.

CONDITIONS

Official Title

Variable-thread Versus Standard Dental Implants for Replacing Missing Teeth

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged more than 18 years.
  • Good general health (ASA I or II, according to the American Academy of Anesthesiology).
  • Require replacement of a posterior single missing tooth with a dental implant.
  • Controlled oral hygiene (full-mouth plaque and bleeding scores 64 25% at baseline).
  • Good compliance and commitment to attend follow-up review appointments.
  • Willing to provide informed consent.
Not Eligible

You will not qualify if you...

  • A healing period of less than four months postextraction at implant site.
  • Localized/generalized periodontitis.
  • Bone metabolic disease and/or taking medications that affect bone metabolism.
  • Long term use of non-steroidal anti-inflammatory medications.
  • History of malignancy, radiotherapy or chemotherapy.
  • Pregnant or lactating women.
  • Severe bruxism or parafunctional habits.
  • Large occlusal discrepancies.
  • Smokers.

AI-Screening

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Trial Site Locations

Total: 1 location

1

MBRU

Dubai, United Arab Emirates

Actively Recruiting

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Research Team

M

Momen Atieh, BDS, MSc, DClinDent, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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