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Parental Satisfaction of Hall Technique for Caries Management in Primary Molars

Parental and Patient Satisfaction of Hall Technique for Caries Management in Primary Molars

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07148401
Enrollment
26
Registered
2025-08-29
Start date
2025-08-25
Completion date
2026-08-30
Last updated
2025-08-29

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

Conditions

Dental Caries

Brief summary

As a newly introduced technique for caries management in primary teeth, patient-centered outcomes such as parental satisfaction, acceptability of the treatment and child discomfort needs to be investigated about Hall technique. Therefore , the aim of our study is to investigate parental and patient satisfaction of Hall technique in managing carious primary molars in children.

Detailed description

Children included are those aged from 4 -10 years old. Children with one or more primary molar with class I and class II carious lesions, with no history of pain, or signs of reversible pulpitis . Patients with signs of irreversible pulpitis as spontaneous pain or pain at night or pathological signs as periapical radiolucency and pathological root resorptions are excluded Method: Patient will receive no local anesthesia or tooth preparation. A proper sized preformed stainless-steel crown will be checked first. Then, the crown will be cemented on the tooth using glass ionomer cement The child is instructed to bite on the crown by means of a cotton roll. Excess cement was cleared immediately using a probe after cementation. Primary outcome: Parent satisfaction : Parents satisfaction will be measured by a 5 point Likert scale with five possible answers: strongly agree, agree, neutral, disagree, and strongly disagree.\[9\] Patient discomfort: Discomfort at time of intervention: The Wong-Baker Faces Pain Scale will be used for assessment Secondary outcomes: Clinical evaluation will be performed at two-week interval, 6 and 12 months including : Absence of adverse signs and symptoms of the carious lesion. Crown evaluation including crown retention.

Interventions

DEVICEHall technique

Hall technique for placement of crowns on carious primary molars

Sponsors

National Research Centre, Egypt
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
4 Years to 9 Years
Healthy volunteers
No

Inclusion criteria

* Children with one or more primary molar with class I and class II carious lesions. * Teeth with no history of pain, or signs of reversible pulpitis

Exclusion criteria

* Teeth with signs of irreversible pulpitis as spontaneous pain or pain at night. * Teeth with signs of non-vitality as presence of sinus or fistula or pathologic mobility. * Teeth with pathological radiographic signs as periapical radiolucency and pathological root resorptions. * Parental refusal for the use of stainless steel crown

Design outcomes

Primary

MeasureTime frameDescription
Parental satisfactionat time of insertion, 2 weeks , 6 months, 1 yearParents satisfaction will be measured by a 5 point Likert scale with five possible answers: strongly agree, agree, neutral, disagree, and strongly disagree

Countries

Egypt

Contacts

Primary ContactLamia K Gadallah, Researcher
lm.khairy@nrc.sci.eg002 01001020605

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026