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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01155154
Other study ID # 09-130
Secondary ID
Status Terminated
Phase N/A
First received June 29, 2010
Last updated November 3, 2014
Start date February 2010
Est. completion date February 2012

Study information

Verified date November 2014
Source State University of New York - Downstate Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Research Question: In emergency department patients with simple hand cuts, do prophylactic antibiotics reduce the risk of wound infections?


Description:

Simple hand lacerations, defined as hand lacerations that do not involve special structures such as bones, tendons, vessels, or nerves, are common in the emergency departments. The exact rate of infection in such wounds is unclear. It is also not clear whether prescribing prophylactic antibiotics reduces the risk of infection in simple hand lacerations. The objective of this randomized double blind controlled study is to: 1. Identify the rate of infection in simple hand lacerations, 2. Identify factors or wound characteristics that increase the risk of infection, and 3. Assess whether prescribing prophylactic antibiotics decreases the risk of infections in such wounds compared to placebo.


Recruitment information / eligibility

Status Terminated
Enrollment 73
Est. completion date February 2012
Est. primary completion date February 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- All adult patients (= 18 years of age) presenting to the ED with simple hand lacerations. Anatomically, lacerations distal to the radial carpal ligament will be considered "hand" lacerations. "Simple" or "uncomplicated" laceration refers to one that does not involve any special tissue (bone, tendon, blood vessel, or nerve).

Exclusion Criteria:

- Immunocompromised patients (cancer, chemotherapy, transplant, HIV/AIDs)

- Current or recent (within two weeks) use of any antibiotics

- Allergy to clindamycin or cephalexin

- Bites (e.g. dog, cat, or human)

- Lacerations resulted from crush injury

- Lacerations involving bone, tendon, blood vessel, or nerve

- Lacerations inflicted more than 12 hours prior to ED visit

- Pregnant or breast-feeding women

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
cephalexin
500 mg (two 250 mg capsules) every 6 hours for 7 days
clindamycin
300 mg of clindamycin (two 150 mg capsules) every 6 hours for 7 days
placebo
Two placebo capsules every 6 hours for 7 days

Locations

Country Name City State
United States Kings County Hospital Center Brooklyn New York
United States State University of New York, Downstate Medical Center Brooklyn New York
United States Staten Island University Hospital Staten Island New York

Sponsors (3)

Lead Sponsor Collaborator
State University of New York - Downstate Medical Center Kings County Hospital Center, Staten Island University Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Participants With Presence of Wound Infection Hand lacerations will be examined 10-14 days after initial wound closure and will be assessed for presence of infection. 2 weeks No