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Influence of Working Length Methods in the Performance of Pulpectomies in Primary Teeth

U

Universidade Federal de Santa Catarina

Status

Unknown

Conditions

Endodontically Treated Teeth

Treatments

Other: Pulpectomies

Study type

Interventional

Funder types

Other

Identifiers

NCT03161639
Universidade Federal SC

Details and patient eligibility

About

Verify, through a randomized double-blinded clinical trial, the influence in the performance of pulpectomies in primary teeth, based on two working length methods, electronic and radiographic.

Full description

Samples will be composed of children between 6 and 9 years of age, with the need for endodontic treatment in primary teeth. They will be submitted to anamnesis, clinical and radiographic exams for identification of eligibility criteria for the study. These patients will be divided randomly into 2 groups: G1 - pulpectomy with working length method performed through radiography (n=100) and G2 - pulpectomy with working length method performed with the aid of an apex locator (n=100). Endodontic treatment will be done by a single trained operator. After definite restoration and final radiography, an evaluation of the obturation quality will be performed by another blinded operator, who will evaluate the appropriate obturation length. The clinical treatment success and the radiographies will also be analyzed during a period of 24 months through clinical and radiographic exams, also by a blinded operator.

Enrollment

64 estimated patients

Sex

All

Ages

6 to 9 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Primary molars teeth with caries or defected restorations associated with signs or symptoms of irreversible pulpal inflammation - spontaneous pain or pulpal necrosis - presence of abscess, fistula, edema, periapical or inter-radicular radiolucency

Exclusion criteria

  • Primary molars teeth previously manipulated, with obliteration of the root canal, with bone reabsorption involving the crypt of the permanent tooth, internal or external pathological or physiological reabsorption involving more then half of the shortest root and unrestorable tooth

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

64 participants in 3 patient groups

Operator 1
No Intervention group
Description:
Perform the pulpectomies except the working length measurement
Operator 2
No Intervention group
Description:
Perform the electronic length measurement of the pulpectomies
Operator 3
Active Comparator group
Description:
Perform radiographic length measurement and final evaluation of the pulpectomies
Treatment:
Other: Pulpectomies

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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