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Evaluation of a Modified Ostectomy and Fenestration in Periapical Surgery

Evaluation of a Modified Ostectomy and Fenestration in Periapical Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090985
Enrollment
Unknown
Registered
2024-10-17
Start date
2021-11-15
Completion date
Unknown
Last updated
2024-10-21

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

Conditions

chronic periapical periodontitis

Interventions

Experimental group: 'Guiding groove' method for osteotomy and fenestration in the periapical surgery
Control group:Conventional osteotomy and fenestration in the periapical surgery

Sponsors

Beijing Stomatological Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged between 18-60 years with no sex predilection. 2. The tooth was diagnosed as chronic periapical periodontitis with an indication for endodontic surgery. 3. Single-rooted incisors, canines and lesion involving a single buccal premolars or molars. 4. CBCT measured the maximum diameter of periapical lesions <10mm. 5. No bone defect on the buccal side or the maximum diameter of bone defect on the buccal side <3mm. 6. Patient consent was obtained.

Exclusion criteria

Exclusion criteria: 1. General contraindications for apical microsurgery; 2. Having uncontrolled diabetes and other systemic diseases; 3. Teeth that cannot be restored due to crown defects and are expected to be non-salvageable; 4. Uncontrolled periodontal disease; 5. Pregnant or lactating women 6. The lesion site is closely related to important anatomical structures (inferior alveolar neural tube, mental foramen, maxillary sinus, etc.). 7. Other oral diseases causing pain; 8. Unwilling to participate in clinical trials or unable to follow up on time. 9. Other situations deemed unsuitable for participation by the researcher.

Design outcomes

Primary

MeasureTime frame
Clinical outcome(Success,Failure);Radiographic outcome (Complete healing,Incomplete healing,Uncertain healing,Unsatisfactory healing);VAS Pain score;

Secondary

MeasureTime frame
VRS Swelling indices;Deviation of root end preparation;

Countries

China

Contacts

Public ContactJinghua Sun

Beijing Stomatological Hospital, Capital Medical University

jinghua.sun@qq.com+86 138 1062 4307

Outcome results

None listed

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