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Comparison of pain in root canal therapy of primary teeth in one or two visit

Comparison of post-operative pain following pulpectomy of vital deciduous teeth in one or two sessions: a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016122231473N1
Enrollment
100
Registered
2017-02-05
Start date
2016-12-10
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Pulp therapy in primary. Pulpitis

Interventions

Intervention 1: Control group:Pulpectomy treatment and insert the SSC in one visit. Intervention 2: Intervention group: Pulpectomy treatment in one session and the second session insert the SSC.
Control group:Pulpectomy treatment and insert the SSC in one visit
Intervention group: Pulpectomy treatment in one session and the second session insert the SSC.

Sponsors

Research and Technology Vice Chancellry, Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 12 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: vital decidious teeth with active bleeding during access cavity preparation,  lack of clinical and radiographic evidence of pulpal necrosis,  resorption of less than two third of the root length, restoration possible, cooperative child, at least one molar with evidence of irreversible pulpitis , e.g. sensitivity to cold or hot stimulus. Exclusion criteria: child with systemic diseases, follicular or dentigerous cyst below decidous tooth, pathologic resorption of at least one third of root length with fistulous sinus tract, resorption of more than two third of root length, isolation of tooth not possible, advanced internal resorption, periradicular lucency involving permanent tooth bud.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain relief after visit. Timepoint: one day-seven days. Method of measurement: VAS.

Secondary

MeasureTime frame
Pain relief. Timepoint: 1-7 day. Method of measurement: VAS.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Masoumeh Aminizadeh

Kerman Univesity of Medical Sciences -School of Dentistry

Aminizadeh66@yahoo.com+98 34 1211 9021

Outcome results

None listed

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