Skip to content

Single-arm clinical trial of a novel intraoperative device for intentional replantation

Single-arm clinical trial of a novel intraoperative device for intentional replantation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083064
Enrollment
Unknown
Registered
2024-04-15
Start date
2023-12-20
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

apical periodontitis

Interventions

Experimental group:Intentional replantation was performed with the use of a digitally assisted device

Sponsors

School and Hospital of Stomatology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 59 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged from 18 to 59 years old 2. Teeth with persistent symptoms due to failure of conventional root canal therapy and apical surgery 3. The proximity of mandibular molars to important anatomical knots makes apical surgery impossible, such as mandibular molars close to the mandibular nerve canal, mandibular premolars close to the mental foramen, and some maxillary teeth close to the maxilla 4. Abnormal root surface groove of lateral incisors reaching to the root apex 5. Refractory apical infection of the mandibular second molar 6. Good compliance, able to participate in the 12-month follow-up 7. Good general condition 8. Written informed consent was obtained

Exclusion criteria

Exclusion criteria: 1. Systemic diseases (diabetes, osteoporosis, heart disease, etc.) 2. Periodontitis with extensive alveolar bone loss 3. Alveolar bone defect in furcation area or large furcation Angle 4. The large area of tooth tissue defect cannot be restored by restoration treatment 5. Teeth with root fracture or apical microfracture 6. Teeth with root canal perforation 7. Teeth with incomplete apical foramina 8. Teeth with root resorption into the middle or crown third of the root 9. Medications that may affect soft tissue status (e.g., warfarin and non-steroidal anti-inflammatory drugs) within one month before treatment 10. Women who are pregnant or preparing to become pregnant 11. Unwillingness to participate in this study

Design outcomes

Primary

MeasureTime frame
accuracy;Operation time;

Secondary

MeasureTime frame
prognostic evaluation;Soft tissue healing;Postoperative pain and swelling;

Countries

China

Contacts

Public ContactLiuyan Meng

School and Hospital of Stomatology

mengliuyan@whu.edu.cn+86 158 2765 2404

Outcome results

None listed

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