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Clinical Efficacy Analysis of Revascularization Using Autologous Venous Blood in lmmature Permanent Teeth

Clinical Efficacy Analysis of Revascularization Using Autologous Venous Blood in lmmature Permanent Teeth

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500105878
Enrollment
Unknown
Registered
2025-07-14
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

1.Irreversible pulpitis of young permanent teeth 2.Acute and chronic periapical periodontitis of young permanent teeth

Interventions

Direct stent therapy with autologous venous blood:None
Conventional apical stent therapy:None

Sponsors

Affiliated Stomatological Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 15 Years

Inclusion criteria

Inclusion criteria: 1.Young permanent teeth aged 8-15 years, clinically and radiologically diagnosed with pulp necrosis or periapical periodontitis; 2.Healthy body, no systemic diseases; 3.Root development is in Nolla stage 7-9; 4.Treatment with autologous venous blood pulp revascularization surgery; 5.Complete preoperative and postoperative medical information (clinical symptoms, signs, imaging data); 6.The patient has good compliance and has been followed up for more than 3 years;

Exclusion criteria

Exclusion criteria: 1.Missing key data in medical records (such as follow-up images and efficacy records); 2.Merge other oral diseases (such as dental trauma, jawbone lesions); 3.Those who did not use parallel projection method for root tip photography and had significant image deviation in imaging examination, which cannot be corrected;

Design outcomes

Primary

MeasureTime frame
Root length;Apical foramen;Root canal wall thickness;

Countries

China

Contacts

Public ContactWang Qiuwei

Affiliated Stomatological Hospital of Nanchang University

839840308@qq.com+86 791 83761512

Outcome results

None listed

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