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. 2013 Mar 28;2013(3):CD003878. doi: 10.1002/14651858.CD003878.pub5

Oh 2006.

Methods Trial design: randomised, parallel group trial
Location: Ann Arbor, USA
Number of centres: one (University of Michigan dental clinic, Ann Arbor, USA)
Recruitment period: not stated
Funding source: not stated
Participants Inclusion criteria: 2 single teeth missing in the anterior maxilla (premolar to premolar) allowing the placement of at least 10 mm long implants with a diameter of 3.8 mm
Exclusion criteria: none specified
Age at baseline: immediate 45.2 ±13.2; delayed 47.3 ±17.8
Gender: immediate M8/F4; delayed M2/F10
Number randomised: 24
Number evaluated: 24
Interventions Comparison: Immediate versus conventional loading
Gp A (n = 12) Immediate loading: Single implants placed with a flapless technique and restored first with acrylic restorations and then 10‐14 days later replaced with cemented metal‐ceramic crowns
Gp B (n = 12) Conventional loading: Single implants placed with a flapless technique and restored with cemented metal‐ceramic crowns after 4 months
Zimmer (Zimmer, Carlsbad, Ca, USA) non‐submerged implants were used
Duration of follow‐up: 6 months
Outcomes Prosthesis/implant failures, probing pocket depths, plaque index, sulcus bleeding index, marginal level of soft tissues, soft tissue thickness, width of the keratinised mucosa, Papilla Index by Jemt 1997
6‐month data used
Notes Sample size calculation: not reported but small sample size noted by the authors as a limitation of this study
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk Reported in the article: "The subjects were randomly assigned to one of two groups: IL (12 patients) or DL (12 patients)"
No reply to letter
Allocation concealment (selection bias) Unclear risk Nothing reported in the article
No reply to letter
Blinding of outcome assessment (detection bias) 
 All outcomes Low risk Reported in the article: "All of the clinical measurements were performed by one calibrated blind examiner at baseline (at the time of implant loading) and at 2, 4, and 6 months after implant loading"
Incomplete outcome data (attrition bias) 
 All outcomes Low risk All data presented
Selective reporting (reporting bias) Low risk All outcomes appear to be presented
Other bias Low risk None detected