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Clinical Trials/ISRCTN58672316
ISRCTN58672316
Completed
未知

Patient perception and clinical effectiveness of an allogeneic cortical sheet versus an autologous laminated bone graft for the treatment of horizontal bone defects: a randomized multicenter clinical trial

ThinkingPerio Research - Periocentrum Bilbao0 sites15 target enrollmentJanuary 28, 2021

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
ThinkingPerio Research - Periocentrum Bilbao
Enrollment
15
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 28, 2021
End Date
September 1, 2023
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
ThinkingPerio Research - Periocentrum Bilbao

Eligibility Criteria

Inclusion Criteria

  • 1\. Informed consent after detailed information
  • 2\. Adults at least 18 years of age
  • 3\. Candidates to receive a bone augmentation for implant placement
  • 4\. Presence of a bone defect (\=2 teeth) with at least 2 mm of mucosa
  • 5\. Keratinized remnant whose bone width is insufficient (\<4 mm) measured on a CBCT\-type scanner
  • 6\. The patient must be periodontally treated at least 1 month before the surgical intervention and in addition to all those oral factors that may affect the treatment

Exclusion Criteria

  • 1\. General contraindications for dental/surgical treatment
  • 2\. Inflammatory or autoimmune disease of the oral cavity
  • 3\. Smokers of more than 10 cigarettes a day
  • 4\. Allergy to collagen and analgesics/anti\-inflammatory NSAIDs
  • 5\. History of cancer in different parts of the body that has required radiotherapy or chemotherapy in the last 5 years
  • 6\. Radiation therapy to the head or neck in the last 5 years
  • 7\. Current medication with immunosuppressants, bisphosphonates or high doses of corticosteroids
  • 8\. Pregnant or nursing women
  • 9\. Women of childbearing age who are not using an effective contraceptive method
  • 10\. Participating in other biomedical research studies in the 24 weeks prior to the start of the study

Outcomes

Primary Outcomes

Not specified

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