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Clinical Evaluation of Packable and Conventional Hybrid Composite Resins in Class I Restorations: three-year results

Clinical Evaluation of Packable and Conventional Hybrid Composite Resins in Class I Restorations: three-year results

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-08000118
Enrollment
Unknown
Registered
2008-06-29
Start date
2005-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

caries

Interventions

group A:TPH Spectrum hybrid composite resin/Xeno III self-e
group B:TPH Spectrum hybrid composite resin/XenoIII self-e

Sponsors

School and Hospital of Stomatology, Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Periodontally sound, vital teeth. Indications for treatment were failed restorations or primary caries; 2. Have at least one pair of premolar or molar necessitating class I restoration or replacement of restoration; 3. Medium cavity size. The cavity extended between one-quarter and no more than one-third of the way up one or more of the cuspal slopes; 4. Have molar supported permanent dentitions free of any edentulous spaces and occlusal interferences of clinical significance; the selected teeth must have proximal contact with adjacent teeth; 5. To be able to provide written informed consent and to comply with all study procedures.

Exclusion criteria

Exclusion criteria: 1. They are included in the evaluation of other restorative materials and systems involving the anterior and /or posterior teeth; 2. There is a history of any adverse reaction to clinical materials of the types to be used in the evaluation; 3. There is evidence of active caries, occlusal parafunctions and/or atypical tooth wear.; 4. There is a history of atypical intrinsic staining if the teeth and any existing tooth-colored restorations; 5. Any patients with medical and /or dental histories which could possibly complicate the provision of the proposed restoration and/or influence the behavior and performance of the restorations in clinical service; 6. Patients who maintain an unacceptable standard of oral hygiene; 7. The opposite tooth of the selected tooth need restoration or replacement of restoration.

Design outcomes

Primary

MeasureTime frame
Anatomical for;

Secondary

MeasureTime frame
postoperative sensitivit;

Countries

China

Contacts

Public ContactChen Zhi
zhichen@whu.edu.cn+86 027 87865051

Outcome results

None listed

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