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Comparison of LSTR and Pulpectomy in Primary Molars of Pediatric Patients (LSTR-PULP)

Comparison of Lesion Sterilization and Tissue Repair Technique With Conventional Pulpectomy in the Treatment of Pulpal Lesions in Primary Molars in Children

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07026435
Acronym
LSTR-PULP
Enrollment
110
Registered
2025-06-18
Start date
2024-08-16
Completion date
2025-11-10
Last updated
2026-05-29

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

Conditions

Dental Caries, Pediatric Dentistry, Periapical Periodontitis, Primary Tooth Pulpectomy, Pulpal Necrosis

Keywords

LSTR, Pulpectomy, Primary teeth, Triple antibiotic paste

Brief summary

This study aims to compare the effectiveness of Lesion Sterilization and Tissue Repair (LSTR) with conventional pulpectomy in treating pulpal lesions in primary molars of pediatric patients aged 4 to 10 years. LSTR is a minimally invasive method that uses antibiotic paste to disinfect infected tissue without full canal instrumentation. Children participating in this study will receive either the LSTR technique or standard pulpectomy, and the clinical and radiographic success of both treatments will be evaluated over a 12-month period. The goal is to determine whether LSTR is a safe and effective alternative to pulpectomy in primary teeth.

Detailed description

This is a prospective, comparative clinical trial conducted at Atatürk University, Department of Pediatric Dentistry, Erzurum, Turkey. The study compares two endodontic treatment methods for primary molars with pulpal lesions in children aged 4 to 10 years. A total of 110 primary molar teeth from 98 pediatric patients were included. Teeth were assigned to two main treatment groups: the experimental group receiving Lesion Sterilization and Tissue Repair (LSTR) and the control group receiving conventional pulpectomy. Each group was further divided into two subgroups based on the type of final restoration - stainless steel crown (SSC) or compomer - resulting in four treatment-restoration combinations: LSTR + SSC, LSTR + compomer, pulpectomy + SSC, and pulpectomy + compomer. Restoration type was determined based on patient cooperation and parental preference. The LSTR group was treated with a combination of ciprofloxacin and metronidazole antibiotics mixed with iodoform-calcium hydroxide paste (Viopex), applied to the canal orifices without mechanical instrumentation. The pulpectomy group received standard chemomechanical canal debridement and obturation with iodoform-calcium hydroxide paste. Both groups were subsequently restored with either SSC or compomer. Patients were followed up clinically and radiographically at 3, 6, and 12 months. Clinical parameters assessed included spontaneous pain, percussion sensitivity, abscess, fistula, and pathological mobility. Radiographic parameters included periapical and interradicular lesion resolution, internal root resorption, and external root resorption. Overall tooth survival was evaluated using Kaplan-Meier survival analysis and Log-Rank test. The primary objective was to assess whether LSTR achieves similar clinical and radiographic success compared to conventional pulpectomy, and to determine the effect of restoration type on long-term treatment outcomes.

Interventions

PROCEDURELSTR

Lesion Sterilization and Tissue Repair (LSTR) is a minimally invasive pulp therapy using ciprofloxacin and metronidazole mixed with iodoform-calcium hydroxide, without canal instrumentation. The access cavity is sealed and restored with SSC or compomer.

PROCEDUREPulpectomy

Pulpectomy includes mechanical canal preparation, irrigation, and obturation using iodoform-calcium hydroxide paste, followed by final restoration with stainless steel crown or compomer.

Sponsors

taymour abuawwad
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
4 Years to 10 Years
Healthy volunteers
No

Inclusion criteria

* Children aged 4 to 10 years. * Presence of at least one primary molar with pulpal involvement requiring endodontic treatment. * Good general health without systemic conditions. * Signed informed consent from parent or legal guardian.

Exclusion criteria

* Children with systemic diseases or immune-compromising conditions. * Known allergies to any of the materials or antibiotics used in the study. * Uncooperative behavior preventing dental treatment under normal clinical conditions. * Teeth with non-restorable crown structure or excessive root resorption.

Design outcomes

Primary

MeasureTime frameDescription
Clinical Success Rate of Treated Primary MolarsAt 3, 6, and 12 months post-treatmentClinical success is defined as absence of pain, swelling, sinus tract, and pathological mobility assessed through standardized clinical examination by a pediatric dentist.

Secondary

MeasureTime frameDescription
Radiographic Healing Rate of Treated Primary MolarsAt 6 and 12 months post-treatmentRadiographic healing is defined as the resolution of periapical or interradicular radiolucency, and the absence of pathological root resorption progression. Radiographic assessment was performed by evaluating the presence or absence of periapical/interradicular lesions, internal root resorption, and external root resorption on digital periapical radiographs. Note: The Periapical Index (PAI) scoring system was originally planned but was not applied due to the radiographic characteristics of primary teeth and the nature of the lesions encountered; descriptive radiographic assessment was used instead."

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORSera DERELİOĞLU, DDS, PhD

Ataturk University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 30, 2026