Clinical trial Recruiting at 1 site Interventional Ages 7 to 10

Bite effects of Hall crowns on baby molars

Official title: Comparative Evaluation of Occlusal Changes Following Hall Technique Crowns in Different Primary Molar Groups: A Randomized Controlled Clinical Trial

Run by Ankara Yildirim Beyazıt University · NCT07134114 · Data updated 2026-11-12

This trial tests whether placing Hall crowns on different primary molars changes a child's bite, using digital intraoral scans to measure differences.

Quick facts

Study typeInterventional
Ages7 Years to 10 Years
SexAll
Enrollment60 (estimated)
SponsorAnkara Yildirim Beyazıt University
Academic / other
Locations1 site (Ankara, Keçiören)
StatusRecruiting
StartedSeptember 15, 2025
Main results expectedJuly 15, 2026
Study endsDecember 15, 2026
Registry record updatedNovember 20, 2025
Trial IDNCT07134114 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Children aged 7–10 in mixed dentition with at least two carious primary molars eligible for the Hall Technique, ASA I–II status, and cooperative behavior (Frankl 3–4) are ideal candidates.

Probably not a fit

Children with skeletal or dental anomalies, uncontrolled dental pain, missing antagonist teeth, or those outside the specified age/behavior criteria are unlikely to benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The study will recruit 60 healthy children aged 7–10 with at least two carious primary molars and good cooperative behavior. One eligible primary molar per child will be randomly selected and patients stratified into four groups by tooth type and jaw (maxillary/mandibular first or second primary molars). Baseline digital intraoral scans will be taken after completion of other dental treatments, then a Hall crown will be placed and occlusal changes will be tracked using digital model analysis. The trial compares the degree and pattern of occlusal adaptation between molar groups to see if tooth position influences bite changes.

Why it matters

Potential benefit: If successful, findings could help dentists predict and manage bite changes after Hall crown placement, improving comfort and treatment planning for children.

How similar studies have gone: The Hall Technique is an established, well-tolerated method for managing carious primary molars, but detailed digital comparisons of occlusal adaptation by specific molar groups are relatively limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

Inclusion Criteria for Participants

* No skeletal or dental anomalies,
* ASA (American Society of Anesthesiologists) physical status classification of I or II ,
* Frankl Behavior Rating Scale score of 3 or 4,
* In the mixed dentition stage,
* Fully erupted permanent first molars in occlusal contact at maximum intercuspation
* No acute dental pain or need for emergency treatment,
* Presence of at least two primary molars with carious lesions scored as 3, 4, or 5 according to the ICDAS (International Caries Detection and Assessment System),
* Presence of an antagonist tooth for the molar planned to receive Hall Technique,
* Provision of verbal and written informed consent by the participant and legal guardian after reading or listening to the consent form and fully understanding its content.

Inclusion Criteria for Tooth

Based on Clinical Examination:

* No history of prolonged pain in response to thermal or chemical stimuli, or spontaneous pain suggestive of irreversible pulpitis,
* No sensitivity to percussion or palpation,
* Absence of both pathological and physiological mobility,
* No signs of swelling, fistula, or discoloration,
* Sufficient remaining tooth structure to retain a preformed stainless steel crown.

Based on Radiographic Examination:

* Radiolucent lesion associated with dental caries located within the outer one-third to two-thirds of the dentin, with a visible band of normal dentin between the lesion and the pulp,
* At least two-thirds of root length present,
* No signs of internal or external pathological or physiological root resorption,
* Intact lamina dura and normal periodontal ligament space,
* No periradicular bone loss surrounding the roots,
* No calcified masses in the pulp chamber.

Exclusion Criteria:

* Individuals with serious systemic or psychological conditions
* Participants who fail to attend follow-up appointments
* Those who exhibit excessive fear or anxiety reactions and are unable to cooperate during treatment

Where it's running

  • Ankara Yıldırım Beyazıt University Faculty of Dentistry
    Ankara, Keçiören, Turkey (Türkiye)
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.