Focal Infection, Dental Clinical Trial
Official title:
Efficacy, Safety and Tolerability of Amoxicillin + Clavulanic Acid (875mg/125mg) Two Times a Day Compared to Clindamycin (150mg) Four Times a Day for 5-7 Days in Treatment of Acute Odontogenic Infection With or Without Abscess
In clinical practice, amoxicillin + clavulanic acid is widely used in the treatment of odontogenic infection. Therefore, this study is designed to generate data to support its use by demonstrating efficacy, safety and tolerability in comparison with clindamycin in subjects with acute odontogenic infections with or without abscess. This will be a two-arm, parallel, comparative, observer blind, randomised study to assess efficacy, safety and tolerability of amoxicillin + clavulanic acid (875mg/125mg) in comparison with clindamycin (150mg) administered for 5-7 days in subjects with acute odontogenic infections with or without abscess. The study will be performed in adult subjects both male and female ≥18 years of age who present with acute odontogenic infections. A total of 472 subjects will be randomized in 1:1 ratio, i.e. 236 subjects in each treatment arm. The treatment duration of the study will be at least 5 days or maximum 7 days depending upon the treatment response. Subjects will be assessed on Day 5 and if Investigator feels the need of continuing the treatment at Day 5 then treatment will be continued till Day 7. For subjects who do not show treatment response on Day 5, assessments will be performed on Day 7.
This two-arm, parallel, comparative, observer blind, randomised study will be performed in
adult subjects both male and female ≥18 years of age who present with acute odontogenic
infection with or without abscess. A total of 472 subjects will be randomised in 1:1 ratio to
get 205 evaluable subjects in each study arm. After obtaining informed consent, subject will
undergo surgical intervention including surgical incisions, drainages, removal of the
involved tooth, debridement, puncture lavage or trephination, if deemed necessary by the
Investigator. These surgical interventions will be performed before the start of study
treatment. On Day 0 after confirming the eligibility, subjects will be randomised to either
of the study arms. The treatment duration of the study will be at least 5 days which may
increase to 7 days, if Investigator feels the need of continuing the treatment at Day 5. In
such cases clinical assessment will be done again at Day 7. Thus the efficacy evaluation will
be performed at baseline (Day 0) prior to study drug administration and on Day 5 and/ or 7.
Safety laboratory evaluations will be performed at Screening Visit and will be repeated at
end of study treatment i.e. either on Day 5 or Day 7. On Baseline, Day 2, Day 5 and/ or Day
7, Visual Analogue Scale (VAS) will be used to measure amount of pain and swelling that a
subject will experience. This scale has numerical ratings from 0 to 10. Zero would mean "No
pain" and 10 would mean "Worst possible pain". The subject will be asked to choose the most
appropriate score on VAS which best describes his/her pain status over last 24 hours. While
using VAS for swelling, zero would mean "No swelling" and 10 would mean "Maximum possible
swelling". The Investigator will choose the most appropriate score on VAS which best
describes subject's swelling.
Sample for microbiological culture will be obtained at the discretion of Investigator while
performing the surgical procedure. When microbiological culture is indicated and feasible,
two sets (each consisting of aerobic and anaerobic media) will be obtained. This sampling
will be done in approximately 80 subjects randomly who will provide consent at Screening. The
sample will be collected and dispatched in appropriate transport medium to the central
laboratory for culture and antibiotic susceptibility.
Protocol waivers or exemptions will not be allowed.
The total duration of each subject's participation will be 6-9 days including Screening
period of 0-1 day (Day -1 to Day 0) and Treatment period of 5-7 days (Day 0 to Day 5-7).
The primary objective of the study is to compare clinical efficacy (cure and improvement) of
both the treatment arms which uses VAS for assessment of pain and swelling. Since the
clinical efficacy parameters are subjective, it is mandatory to keep the
observer/Investigator blinded during the study assessment. In addition, designing blinded
study is challenging owing to different dosage regimen and formulation of study drugs. The
study design of double blind double dummy is not recommended in view of increased pill burden
which in turn can have an impact on treatment compliance. The possibility of
over-encapsulation is ruled out due to large pill size of amoxicillin + clavulanic acid.
Therefore to maintain blinding of Investigators, the study is designed as observer blind with
Investigator remaining blinded throughout the study period. An unblinded study team member
will be appointed for each site who will be involved in dispensing of the study drugs to
subjects. The unblinded study team member will remain present during subject assessment for
all study visits and will ensure that Investigator remains blinded to treatment assignment.
Study treatment includes amoxicillin + clavulanic acid (875mg/125mg) two times daily or
clindamycin (150mg) four times daily for 5-7 days both administered orally with meal.
Augmentin™ (amoxicillin + clavulanic acid) from GSK and Dalacin-C (clindamycin) from Pfizer
will be used as study treatments. The contents of the label will be in accordance with all
applicable regulatory requirements.
Patients can receive additional medical therapy such as analgesics or anti-inflammatory
drugs. However, opioid analgesics and any other antibiotic apart from study drugs will not be
permitted during entire study period.
This study will be conducted in accordance with ICH GCP, all applicable subject privacy
requirements, and the ethical principles that are outlined in the Declaration of Helsinki
2008, including IRB/ IEC review and approval of study protocol and any subsequent amendments,
subject informed consent and Investigator reporting requirements.
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| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Withdrawn |
NCT04057014 -
Immediate Versus Delayed Treatment of Odontogenic Infections
|
Phase 4 |