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The Efficacy and Safety of Pulp Regeneration Induced by SHED Polymerization

F

Fifth Affiliated Hospital of Guangzhou Medical University

Status

Not yet enrolling

Conditions

Pulp Necroses

Treatments

Drug: Allogeneic human pulp mesenchymal stem cells mixed with hyaluronic acid polymers

Study type

Interventional

Funder types

Other

Identifiers

NCT05728346
Xueli Mao

Details and patient eligibility

About

Dental pulp necrosis is one of the most common pathological conditions that results in tooth loss. However, regeneration of functional dental pulp has proved difficult. Therefore, the investigators conduct a single-arm study to evaluate the efficacy and safety of pulp regeneration induced by SHED mixed with hyaluronic acid polymerization in patients with pulp necrosis of permanent teeth.

Full description

This study is a single-center, prospective, single-arm study to evaluate the efficacy and safety of pulp regeneration induced by SHED mixed with hyaluronic acid polymerization in patients with pulp necrosis of permanent teeth. This study plans to include 30 subjects from the Department of Stomatology of the Fifth Affiliated Hospital of Guangzhou Medical University. All participants in this study will receive stem cells from human exfoliated deciduous teeth (SHED) mixed with hyaluronic acid polymers after the preparation and disinfection of the root canal of the affected teeth. All participants will undergo screening and baseline visits. After surgery, the participants will be followed up for 2 years.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients aged 18 to 45 years
  • Patients with pulp necrosis of a single canal permanent tooth due to trauma or caries
  • Patients who have signed informed consent

Exclusion criteria

  • Patients with pulp necrosis caused by severe trauma to the tooth, such as crown root fracture, tooth root fracture, tooth displacement, etc
  • Patients with calcification of the apical foramen at the root of the tooth
  • History of hereditary disorders of abnormal tooth development
  • Dental occlusal trauma, bruxism, malocclusion
  • Bad oral habits (sticking out the tongue, biting lips, biting nails, sucking fingers, etc.)
  • Presence of uncontrollable pathological processes in the oral cavity (presence of acute advanced diseases in the oral cavity)
  • Malnutrition (serum albumin concentration<2 g/dl)
  • Patients with history of other systemic, communicable or hereditary diseases have been diagnosed
  • Pregnant, nursing, planning to become pregnant
  • The investigators determined that the patient was not suitable for the study

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

single-arm
Experimental group
Treatment:
Drug: Allogeneic human pulp mesenchymal stem cells mixed with hyaluronic acid polymers

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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