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Clinical Trials/NCT02770846
NCT02770846
Completed
Not Applicable

Evaluation of Immediate Loading Versus Delayed Loading in Single-implant Restorations

Folktandvården Skåne AB1 site in 1 country50 target enrollmentApril 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Immediate Dental Implant Loading
Sponsor
Folktandvården Skåne AB
Enrollment
50
Locations
1
Primary Endpoint
Oral Health Impact Profile 14
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The purpose of this prospective randomized clinical study was to compare implant survival, patient satisfaction, and radiographic, clinical, and aesthetic outcomes following immediate loading (IL) and delayed loading (DL) of single dental implants after 1,3 and 5 years of follow-up.

Detailed Description

Purpose: The objective of the present prospective randomized clinical study was to compare the overall treatment outcome following immediate loading (IL) and delayed loading (DL) of single implants after 5 year of follow-up. Patients with a missing maxillary tooth (15-25) were randomly assigned to IL or DL. The protocol included implant installation in healed sites, immediate loading, delayed loading, temporary screw-retained restoration, and replacement with a permanent single implant crown. Outcome measures were implant survival, marginal bone level, soft tissue changes, papillae index, pink, and white esthetic score (PES and WES), patient judged aesthetics, and oral health impact profile (OHiP-14).

Registry
clinicaltrials.gov
Start Date
April 2011
End Date
December 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Folktandvården Skåne AB
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients of at least 18 years of age.
  • In need of one or more single-tooth replacements.
  • The single-tooth replacement needs to be in the anterior maxilla
  • Minimum of mesial-distal width of interdental space of 6 mm

Exclusion Criteria

  • General contraindications for oral surgery
  • Inadequate oral hygiene
  • Insufficient bone volume at the recipient site

Outcomes

Primary Outcomes

Oral Health Impact Profile 14

Time Frame: Pre-surgery

The Oral Health Impact Profile 14 (OHIP-14) measure oral health related quality of life. The oral health-related quality of life is calculated using the Swedish validated version of the Oral Health Impact Profile (OHIP-14) questionnaire. The questionnaires are completed at the beginning of the treatment and 12 months after the definitive crown placement. The scale consists of 14 variables that are scored 1,2,3,4 or 5, the 14 variables scores are combined. Scale range 14-70, 14 minimum and 70 maximum. A low score represent a better oral health related quality of life.

White Esthetic Score

Time Frame: 5 years

The White esthetic score (WES) measures the aesthetic appearance of the implant crown. Intraoral photographs from the aesthetic baseline and follow-up appointments are used to register the white esthetic score, an objective aesthetic scale were the shape,size,colour and structure of the implant crown is rated. The scale consists of 5 variables that are scored 0,1 or 2, the 5 variables scores are combined. Scale range 0-10, 0 minimum and 10 maximum. A higher score represent a better aesthetic outcome.

Oral Health Impact Profile 14 (OHIP-14)

Time Frame: After 12 months

The Oral Health Impact Profile 14 (OHIP-14) measure oral health related quality of life. The oral health-related quality of life is calculated using the Swedish validated version of the Oral Health Impact Profile (OHIP-14) questionnaire. The questionnaires are completed at the beginning of the treatment and 12 months after the definitive crown placement. The scale consists of 14 variables that are scored 1,2,3,4 or 5, the 14 variables scores are combined. Scale range 14-70, 14 minimum and 70 maximum. A low score represent a better oral health related quality of life.

Change in Level of Marginal Bone

Time Frame: Baseline to 5 years

Digital intra-oral periapical radiographs at different time points. The marginal bone level is measured after calibration. Measurements are taken from the implant-abutment junction to the marginal bone level (millimetres). Change in marginal bone level is calculated by comparing bone-to-implant contact level of all appointments to radiographic baseline.

Pink Esthetic Score

Time Frame: After 5 year

The Pink esthetic score (PES) measures the aesthetic appearance of mucosa tissue at the implant site. Intraoral photographs from the aesthetic baseline and follow-up appointments are used to register the pink esthetic score, an objective aesthetic scale were the shape,size,colour and structure of the soft tissue is rated. The scale consists of 7 variables that are scored 0,1 or 2, the 7 variables scores are combined. Scale range 0-14, 0 minimum and 14 maximum. A higher score represent a better aesthetic outcome.

Study Sites (1)

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