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clinic outcomes of NobelParallel CC short implants in posterior atrophic edentulous mandibles

Single tooth reconstructions supported by NobelParallel Conical Connection Short implants vs conventional implants with augmentation in atrophic posterior mandibles: A 1-year prospective study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042139
Enrollment
Unknown
Registered
2021-01-14
Start date
2021-01-01
Completion date
Unknown
Last updated
2021-04-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dentition Defect

Interventions

short implant group:placement of short implant
conventional implant group:placement of conventional implant

Sponsors

The Affiliated Hospital of Stomatology, School of Stomatology, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patient aged >=18 years and sign the informed consent; 2.loss of single tooth in posterior mandible(molar or premolar), in need for one implant; 3.There is vertical resorption at tooth loss site and the vertical height of residual ridge is 7-10 mm; 4.Horizontal width of the residual bone at the tooth loss site >= 6mm; 5.Patient recieve treatment involving the placement of a NobelParallel CC short implants (7 or 8.5 mm) in the native bone or standard-length implants (>= 10 mm) in ridges augmented; 6.a follow-up period of 1 year from final restoration.

Exclusion criteria

Exclusion criteria: 1.General contraindications to implant surgery; 2.subjected to irradiation in the head and neck area within two years prior to treatment; 3.benign or malignant tumors in the area intended for implant placement; 4.treated or under treatment with intravenous amino-bisphosphonates; 5.untreated periodontitis; 6.poor oral hygiene and motivation(median of full mouth plaque index >=2); 7.uncontrolled diabetes(HbA1c>8.0% or FBG>150mg/dl); 8.pregnant or nursing; 9.psychiatric problems; 10.lack of opposite occluding dentition in the area intended for implant placement; 11.acute or chronic infection/inflammation in the area intended for implant placement; 12.extraction sites with less than 3 months of healing; 13.heavy smoking(>20 cigarettes/day).

Design outcomes

Primary

MeasureTime frame
marginal bone level;implants survival rate;prosthetics survival rate;patient-reported outcome;implant stability quotient;modified plaque index;gingival bleeding index;peri-implant probing pocket depth;

Countries

China

Contacts

Public ContactHe Fuming

The Affiliated Hospital of Stomatology, School of Stomatology, Zhejiang University School of Medicine

hfm@zju.edu.cn+86 13516817697

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026