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Clinical Trials/IRCT20210330050791N1
IRCT20210330050791N1
Completed
未知

Clinical comparison of coronally advanced flap plus amniotic membrane seeded with whartons' jelly mesenchymal stem cells and subepithelial connective tissue graft in the treatment of single Miller's class I and II gingival recessions

Shiraz University of Medical Sciences0 sites20 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Shiraz University of Medical Sciences
Enrollment
20
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients aged 18 or more
  • Patients who have read, understood, and signed an informed consent form
  • Patients who have been able and willing to follow study procedures and instructions
  • Patients who have at least one tooth with buccal Miller class I or II recession type defects
  • Recessions with \= ? mm depth and \= ?mm width in premolar, canine or incisor area, with probing depths \=? mm and \= ? mm keratinized tissue
  • Treating only one tooth at each side as a test or control tooth in case of adjacent teeth with recession defects

Exclusion Criteria

  • ?ubjects who are participating in other clinical trials
  • Subjects who have a history of cancer or human immunodeficiency virus
  • Subjects who have an uncontrolled systemic disease with compromised healing potential (such as diabetes mellitus with a recent HbA?c \> ?%)
  • Using medications known to cause gingival enlargement and anticoagulants with International Normalized Ratio (INR) \> ?.? and taking herapeutic doses of medications known to affect bone metabolism
  • Those who fail to maintain good plaque control
  • Teeth with extremely prominent root surfaces
  • Teeth with Class V restorations extending to root surfaces
  • Subjects who have any systemic acute infections in the areas intended for surgery
  • Female subjects who are pregnant or lactating
  • History of surgical periodontal treatment of the involved site

Outcomes

Primary Outcomes

Not specified

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