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Clinical Trials/KCT0008393
KCT0008393
Completed
未知

Healing pattern of peri-implant dehiscence defects around implants with chemically modified SLA surface: A randomized controlled clinical trial

Yonsei University Health System, Dental Hospital0 sites50 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Yonsei University Health System, Dental Hospital
Enrollment
50
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
June 10, 2021
Last Updated
2 years ago
Study Type
Interventional Study
Sex
All

Investigators

Sponsor
Yonsei University Health System, Dental Hospital

Eligibility Criteria

Inclusion Criteria

  • 1\. Periodonally healthy adult men and women aged 18 years or older
  • 2\. Good oral hygiene (plaque index \<25% in the entire jaw) (O'Leary et al. 1972\)
  • 3\. The level of inflammation control is adequate (bleeding on probing of the anterior jaw \<25%) (Ainamo \& Bay 1975\)
  • 4\. Those who need to place 1 or 2 implants in the edentulous area where 1 or 2\-3 teeth are continuously lost
  • 5\. A person who has one or more dehiscence defects of 3 mm or more in the apico\-coronal direction around the fixture after implant placement
  • 6\. A person who can achieve sufficient fixation during implant placement (determined during implant surgery)
  • 7\. If more than 3 months have passed since tooth extraction
  • 8\. Cases where soft tissue transplantation is not required after implant placement

Exclusion Criteria

  • 1\. A person who has undergone hard tissue or soft tissue transplantation within the last 6 months
  • 2\. Those who smoke more than 10 cigarettes a day
  • 3\. Drugs that cause soft tissue hypertrophy (e.g., diuretics, immunosuppressants, antiepileptics) or drugs that interfere with bone formation (e.g., corticosteroids) within 2 weeks of screening, or may be taken during the clinical trial person with
  • 4\. Those who have administered oral or injection rheumatism treatment within 2 weeks from the time of screening
  • 5\. Patients with uncontrolled diabetes or hypertension
  • 6\. Those with skin diseases or lesions in the oral cavity (e.g., erosive lichen planus, erosive lichen planus, stomatitis, ulcers, malignant tumors)
  • 7\. Those suffering from systemic diseases related to bone metabolism such as osteomyelitis
  • 8\. Those who have been or are currently taking oral or injectable bisphosphonate medicines for osteoporosis for more than 3 months (However, according to AAOMS, those who have stopped taking medication for more than 3 months and have CTx level of 0\.150ng/ml or higher participate in clinical research) possible)
  • 9\. Those who have a history of tumor removal at the surgical site
  • 10\. Subjects with Full Mouth Plaque Score and Full Mouth Bleeding Score of 25% or higher

Outcomes

Primary Outcomes

Not specified

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