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Comparison of non pharmacological methods in reducing complications of the primary teeth eruption

Comparison of effectiveness of non-pharmacological and herbal treatments in reducing complications of the primary teeth eruption in children 5 to 15 months

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201211127402N3
Enrollment
450
Registered
2012-11-26
Start date
2012-12-21
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

Complications of the primary teeth eruption. Disturbances in tooth eruption

Interventions

Intervention 1: 1. Eruption Control: no specific treatment is done and behavioral therapy is used only. Intervention 2: 2. Nonpharmacologic treatments: the group is trained with the distribution of pa
Behavior
Treatment - Other
1. Eruption Control: no specific treatment is done and behavioral therapy is used only.
2. Nonpharmacologic treatments: the group is trained with the distribution of pamphlets on primary teeth eruption and potential problems within it. Also to treat symptoms of tooth eruption, nonpharmac
3. Herbal treatments: the group is trained with the distribution of pamphlets on primary teeth eruption, Herbal treatments of eruption symptoms are taught to parents such as licorice root for chewing

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 2 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Normal birth weight (= 2500 g); Fullterm and healthy neonates; with at least one primary teeth not erupted. Exclusion criteria: Children with infectious diseases; Syndromic children; Children with systemic diseases.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Fever. Timepoint: Beginning of the research, Fourth day, Eighth day, Eleventh day. Method of measurement: Thermometer, Questionnaires, Physical examination, Observation.;Pain. Timepoint: Beginning of the research, Fourth day, Eighth day, Eleventh day. Method of measurement: , Questionnaires, Physical examination, Observation.;Drooling. Timepoint: Beginning of the research, Fourth day, Eighth day, Eleventh day. Method of measurement: Questionnaires, Physical examination, Observation.;Diarrhea. Timepoint: Beginning of the research, Fourth day, Eighth day, Eleventh day. Method of measurement: Questionnaires.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahtab Memarpour

Shiraz University of Medical Sciences

memarpour@sums.ac.ir+98 71 1626 3192

Outcome results

None listed

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