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NCT Number: NCT07810244

Moxifloxacin Versus Clindamycin in the Management of Odontogenic Maxillofacial Infectious Processes

We are conducting a trial to compare moxifloxacin against clindamycin for dental infections that spread to the face and jaw. The study will enroll 60 adults who are being treated as outpatients for localized abscesses or cellulitis. Every patient will first receive minor surgical drainage in the clinic. Following drainage, they are randomly assigned to take either moxifloxacin (400 mg once daily) or clindamycin (300 mg four times daily) for 5 to 7 days.

Our primary focus is early pain relief. We will measure the drop in pain scores using a 100 mm visual scale at the day 2-3 follow-up visit. We also plan to track how many patients are fully cured by day 5-7, monitor any side effects, and test the infection samples to see exactly which bacteria are present and how they respond to both drugs.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Nishtar Institute of Dentistry Multan

Multan, Punjab Province, 60000, Pakistan

Location contact

Dr. Sohail Fareed, FCPS (OMFS)

CONTACT

[email protected]

+923017430431

Zeeshan Aslam, FCPS Resident (OMFS)

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged 18 years and above of either gender presenting to the Outpatient Department of the Nishtar Institute of Dentistry, Department of Maxillofacial Surgery.
  • Clinical and radiographic diagnosis of an odontogenic maxillofacial infection - gingival inflammatory infiltrate or a localized abscess/cellulitis (ICD-10: K04, K05) - manageable on an outpatient basis with minor office-based surgical drainage (incision/drainage, extraction, or trepanation under local anaesthesia) and adjunctive oral antibiotic therapy, not requiring hospital admission.
  • Patients providing written informed consent for participation.

Exclusion criteria

  • Known hypersensitivity to fluoroquinolones, lincosamides, or cephalosporins.
  • Pregnant or lactating women.
  • Patients with diabetes mellitus, known HIV infection, hepatic dysfunction, or renal impairment (creatinine clearance < 50 mL/min).
  • Patients with known cardiac arrhythmia, bradycardia, electrolyte imbalance (particularly hypokalaemia), or a history of tendinopathy related to quinolone use.
  • Patients with signs of a severe or spreading systemic infection (e.g., extensive facial/neck swelling, trismus, dysphagia, or high-grade fever) requiring hospital admission, intravenous antibiotics, or extraoral surgical drainage under general anaesthesia.
  • Patients who received systemic antibiotic therapy within the preceding 7 days.

Treatment and study plan

Clindamycin

Drug

Clindamycin 300 mg oral capsule, four times daily.

Moxifloxacin (400 mg)

Drug

Moxifloxacin 400 mg oral tablet, once daily.

Primary outcomes

  1. clinical cure rate

    Time frame: 5-7 days

    To compare the clinical cure rate (complete resolution of signs and symptoms) at the end of treatment (day 5-7) between the two groups.

  2. pain intensity

    Time frame: 2-3 days

    To compare the mean percentage reduction in pain intensity (VAS) at day 2-3 from baseline between patients treated with moxifloxacin and patients treated with clindamycin.

Study contacts

Contact information is provided by the study sponsor or research team.

Zeeshan Aslam, FCPS R(OMFS)

CONTACT

[email protected]

+923238632670

Sponsors and collaborators

Lead sponsor

Nishtar Medical University

Other

Registry information

Official study title

Moxifloxacin Versus Clindamycin in the Management of Odontogenic Maxillofacial Infectious Processes: A Preliminary, Intrahospital, Controlled Clinical Trial

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Sep 9, 2026
Registry last updated
Sep 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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