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Appropriate use of antibiotics in the perioperative period for jaw deformity related intervention research

Appropriate use of antibiotics in the perioperative period for jaw deformity related intervention research - Intervention study of antibiotic use in jaw deformity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000054228
Enrollment
120
Registered
2024-04-23
Start date
2024-04-23
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

jaw deformity

Interventions

This study does not use any special test drugs or equipment. Cefazolin sodium for injection (CEZ) used, the route of administration is intravenous injection, and the single dose is 1 g. Single intra

Sponsors

Tohoku University Graduate School of Dentistry
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The subjects were cases in which maxillary and maxillary osteotomies (2 jaw surgery) were indicated in the preoperative evaluation. In addition, subjects with no signs of inflammation or symptoms in the jawbone area before surgery were included.

Exclusion criteria

Exclusion criteria: (Exclusion to affect effectiveness evaluation) (1) Patients with diabetes or blood diseases (2) Patients with inflammatory findings in the jawbone area, risk of infective endocarditis (IE), and risk of drug-induced osteonecrosis of the jaw (MRONJ) (3) Patients taking steroids or immunosuppressive drugs (4)Patients participating in other studies (Exclusion to affect safety assessment) (4) Patients with allergies to cephem antibiotics (5) Patients who are taking anticoagulants, antithrombotic drugs, etc. and are at risk of bleeding (6)Patients with renal dysfunction (7) Women who are pregnant, may become pregnant, within 28 days after giving birth, or are breastfeeding. (Exclusion from the perspective of risk/benefit balance) (8) Patients who are judged to be difficult to participate in research due to psychosis or psychiatric symptoms

Design outcomes

Primary

MeasureTime frame
The following items on the 1st, 3rd, 7th, 14th, and 28th days after surgery Presence or absence of fever, presence or absence of cheek swelling, painless mouth opening, pain score (NRS), presence or absence of wound swelling, presence or absence of wound drainage.

Countries

Japan

Contacts

Public ContactYushi Ezoe

Tohoku University Graduate School of Dentistry Division of Oral and Maxillofacial Surgery

geka0329@dent.tohoku.ac.jp0227178350

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026