CompletedPhase 2/3

Lesion Sterilization And Tissue Repair Versus Zinc Oxide And Eugenol For Treatment of Necrotic Primary Molars

Egypt60 participantsStarted 2022-10-01

Plain-language summary

The aim of this study is to evaluate the clinical and radiographic success of Lesion Sterilization And Tissue Repair \[ LSTR\] antibiotic paste versus Zinc Oxide and Eugenol pulpectomy in the treatment of non-vital primary molars.

Who can participate

Age range

5 Years – 7 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Aged between 5 years and 7 years.
. With deep caries involving pulp in primary molars.
. Necrotic teeth with or without periapical or furcal lesions.
. Primary molars with minimal root resorption not more than 1/3 of root.

Exclusion criteria

. Children with systemic disease
. Previous history of allergy to antibiotics used in the study.
. Children that will not attend follow up.
. Caries in primary teeth exhibiting pre-shedding mobility.
. Non restorable teeth.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Post oper3tive pain

Timeframe: 1 month

Post operative pain

Timeframe: 3 months

Post operative pain

Timeframe: 6 months

Tenderness

Timeframe: 1 month

Tenderness

Timeframe: 3 months

Tenderness

Timeframe: 6 months

Swelling /sinus tract or fistula

Timeframe: 1 month

Swelling /sinus tract or fistula

Timeframe: 3 months

Trial details

NCT IDNCT05448937

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-10-01

View on ClinicalTrials.gov More Necrotic Primary Molars trials

Who can participate

Age range

5 Years – 7 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Aged between 5 years and 7 years.
. With deep caries involving pulp in primary molars.
. Necrotic teeth with or without periapical or furcal lesions.
. Primary molars with minimal root resorption not more than 1/3 of root.

Exclusion criteria

. Children with systemic disease
. Previous history of allergy to antibiotics used in the study.
. Children that will not attend follow up.
. Caries in primary teeth exhibiting pre-shedding mobility.
. Non restorable teeth.

What they're measuring

Post oper3tive pain

Timeframe: 1 month

Post operative pain

Timeframe: 3 months

Post operative pain

Timeframe: 6 months

Tenderness

Timeframe: 1 month

Tenderness

Timeframe: 3 months

Tenderness

Timeframe: 6 months

Swelling /sinus tract or fistula

Timeframe: 1 month

Swelling /sinus tract or fistula

Timeframe: 3 months