Post Operative Pain Following Pulpectomy Versus Pulpotomy in Primary Molars Wit Irreversible Pulpitis

Study will evaluate and compare post operative pain for primary molars with irreversible pulpitis after pulpotomy and pulpuectomy

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Key information

Conditions

Irreversible Pulpitis

Age range

4 year–10 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Healthy individual
Has primary tooth with irreversible pulpitis
Cooperative child

Exclusion criteria

Mentally, physically or medically compromised children
Uncooperative children

Treatment and study plan

Non vitalPulp therapy

Other

Pulp therapy deals about management of inflamed vital dental pulp With complete pulp removal and obturation with resorbable materi

Vital pulp therapy

Other

Pulp therapy through partial root removal and using of regenerative capping material

Primary outcomes

Post operative pain

Time frame: 6 months

Post operative pain using pain scale after 1,2,7 days

Sponsors and collaborators

Lead sponsor

Minia University

Other

Registry information

Official study title

Post Operative Pain Following Pulpectomy Versus Pulpotomy in Primary Molars Wit Irreversible Pulpitis a Parallel Randomized Clinical Trial

Important dates

Study start: 2025
Primary completion: 2025
Study completion: 2025
First posted: Mar 30, 2025
Registry last updated: Mar 30, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

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