UnknownNot Applicable

Micro-invasive Methods of Mid-palatal Sutural Separation

27 participantsStarted 2023-03-20

Plain-language summary

This trial aims to evaluate the effect of different micro-invasive methods (piezoelectric and micro-osteoperforation) along with tooth-tooth borne RPE compare to tooth-bone borne MARPE on the amount of mid-palatal sutural separation in late adolescent patients. Null Hypothesis There is no effect of adjunctive micro-invasive methods (piezoelectric and microosteoperforation) on mid-palatal suture separation with tooth-tooth borne RPE appliance compared to tooth-bone borne MARPE

Who can participate

Age range14 Years – 20 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓. Patients with the bilateral maxillary transverse deficiency.
✓. Patient referred by orthodontists for SARME or MARPE.
✓. Patients with developmental age in stage C or stage D maturation stages .
✓. Patients without developmental deformity.
✓. Good oral hygiene.
✓. Patient with intact maxillary first premolars and first molars.

Exclusion criteria

✕. Congenital maxillofacial deformities mainly cleft patients.
✕. Previous orthodontic and surgical treatment on the maxilla.
✕. Maxillary trauma.
✕. Previous extraction in the maxillary arch.
✕. Patients with periodontal disease.

What they're measuring

Intraoral scanner outcomes

Timeframe: T0: before expansion

Intraoral scanner outcomes

Timeframe: T1:3 months after expansion

Intraoral scanner outcomes

Timeframe: T2: 6 months after expansion

CBCT Outcomes

Timeframe: T0: before expansion

CBCT Outcomes

Timeframe: T1:3 months after expansion

CBCT Outcomes

Timeframe: T2:6 months after expansion.

Trial details

NCT IDNCT05740592

SponsorUniversity of Baghdad

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-08-20

Contact for this trial

Hayder A. Naseri, Ph.D. student

009647726146182 dr.haideraaa@gmail.com

View on ClinicalTrials.gov More Maxillary Expansion trials

Plain-language summary

Who can participate

Age range14 Years – 20 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓. Patients with the bilateral maxillary transverse deficiency.
✓. Patient referred by orthodontists for SARME or MARPE.
✓. Patients with developmental age in stage C or stage D maturation stages .
✓. Patients without developmental deformity.
✓. Good oral hygiene.
✓. Patient with intact maxillary first premolars and first molars.

Exclusion criteria

✕. Congenital maxillofacial deformities mainly cleft patients.
✕. Previous orthodontic and surgical treatment on the maxilla.
✕. Maxillary trauma.
✕. Previous extraction in the maxillary arch.
✕. Patients with periodontal disease.

What they're measuring

Intraoral scanner outcomes

Timeframe: T0: before expansion

Intraoral scanner outcomes

Timeframe: T1:3 months after expansion

Intraoral scanner outcomes

Timeframe: T2: 6 months after expansion

CBCT Outcomes

Timeframe: T0: before expansion

CBCT Outcomes

Timeframe: T1:3 months after expansion

CBCT Outcomes

Timeframe: T2:6 months after expansion.