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Restoration of dental pulp using hydrogel

Regeneration of dental pulp complex in closed apex necrotic teeth using fibrin hydrogel.

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230513058168N1
Enrollment
10
Registered
2023-06-11
Start date
2023-05-14
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

teeth with with irreversible pulpitis. Pulpitis

Interventions

Intervention 1: Intervention group: Suggested root canal treatment intervention using 1 million cord stem cells in 300 microliters of fibrin hydrogel containing 300 micrograms of exosome and growth f

Sponsors

University of San Francisco
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients must be systemically healthy, Class I dental category Involved teeth must have no periodontal disease detectable by periodontal examination. Patients must present with radiographic signs of endodontic disease (i.e., necrotic pulp with periapical radiolucency) One-rooted teeth number ?, ? and ? with irreversible pulpitis (need root canal treatment)".

Exclusion criteria

Exclusion criteria: Presence of any disease or medication that alters the immune system or interferes with healing ability Smokers (more than ?? cigarettes per day) External or internal tooth resorption Tooth perforation from the pulp cavity through the tip of the root exposing the tissue to material in the oral cavity. Pregnant or nursing mothers because hormonal factors may influence the condition. Allergies or adverse reactions to local anesthetic medications Patients under the age of ?? Patients with an ASA Classification II or higherI. Cardiovascular Disease Disable or mental illness Osteoporosis

Design outcomes

Primary

MeasureTime frame
Radiographic observations. Timepoint: Before the intervention and 1 week, 3 months and 6 months after the intervention. Method of measurement: Radiographic observations.;Examination of signs of apical healing and dental vital signs. Timepoint: Before the intervention and 1 week, 3 months and 6 months after the intervention. Method of measurement: Routine dental vital test methods.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNeda Bayat

Tehran University of Medical Sciences

bayat.neda@yahoo.com+98 21 4305 2000

Outcome results

None listed

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