Recruiting NA Bone Resorption

Compares treatment options for Bone Resorption

Official title Guided Bone Regeneration Using Fixed vs Non-Fixed Resorbable Collagen Membranes

ClinicalTrials.gov ID: NCT06334159

What this study is testing

What it's testing
The aim of this clinical trial is to compare the horizontal bone gain when grafting a bone substitute with non fixed resorbable collagen membranes (control group), versus fixed resorbable collagen membranes (test group) in resorbed ridges requiring Guided Bone Regeneration (GBR) to facilitate implant placement at 6 months.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 and older. Healthy volunteers may be eligible.

You may be able to join if

  • Men and women over 18 years old or older
  • Patients requiring Guided Bone Regeneration due to insufficient ridge width(≤5mm) to place dental implants, with sufficient vertical ridge height...
  • One or more teeth missing in posterior zone (Premolars, and Molars)
  • Absence of active Periodontal disease
  • Good level of oral hygiene (Plaque index \<25%)

You likely can't join if

  • Patients with sufficient ridge width (\>5 mm) and height (≥9mm) from vital anatomical structure) requiring no GBR to place dental implants
  • Patients with severe horizontal and vertical defects requiring other surgical techniques.
  • Long-term non-steroidal anti-inflammatory drug therapy (3months).
  • Lactating females or currently pregnant women.
  • Severe cognitive or psychiatric disorders.
  • Unwillingness to return for follow-up examination.
See the full eligibility criteria
Who can join
  • Men and women over 18 years old or older
  • Patients requiring Guided Bone Regeneration due to insufficient ridge width(≤5mm) to place dental implants, with sufficient vertical ridge height (≥9mm) from vital anatomical structures (the inferior alveolar nerve in...
  • One or more teeth missing in posterior zone (Premolars, and Molars)
  • Absence of active Periodontal disease
  • Good level of oral hygiene (Plaque index \<25%)
  • Absence of systemic diseases that could influence the outcome of the therapy (Uncontrolled diabetes, osteoporosis, bisphosphonate medications)
  • Non smokers or light smokers (\<10 cigarettes per day)
  • Informed consent signed
What rules you out
  • Patients with sufficient ridge width (\>5 mm) and height (≥9mm) from vital anatomical structure) requiring no GBR to place dental implants
  • Patients with severe horizontal and vertical defects requiring other surgical techniques.
  • Long-term non-steroidal anti-inflammatory drug therapy (3months).
  • Lactating females or currently pregnant women.
  • Severe cognitive or psychiatric disorders.
  • Unwillingness to return for follow-up examination.

The study team makes the final eligibility decision.

Where it's taking place

  • Barcelona, Sant Cugat Del Vallès, Spain

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Barcelona, Sant Cugat Del Vallès, Spain. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.