CClinicalTrials.gg
CompletedNCT01899781Updated Feb 17, 2020

Prophylactic Antibiotic Treatment for Hand Lacerations Involving Flexor and/or Extensor Tendon

A Phase 4 interventional study of Antibiotic-Cefamezin in Hand Laceration, Tendon Involved and Clean Laceration, sponsored by HaEmek Medical Center, Israel. Completed. Open to participants aged 13 Years to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-02-17.

Sponsored by HaEmek Medical Center, Israel · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
24
Allocation
Not applicable
Ages
13 Years to 75 Years
Sex
All
01

Study summary

The investigators assume that simple hand lacerations involving flexors or extensors tendons, do not require prophylactic antibiotic treatment to prevent wound infection.

Read the detailed description

Hand lacerations are divided to "complicated" which involves tendons, nerves, bones, and joints, and "simple" which involves only cutaneous and subcutaneous tissue.

prophylactic antibiotic should not be given in a clean simple lacerations, and should be given when a bone is involve (open fracture). But there is not enough data, weather prophylactic antibiotic treatment should be given when only tendons are involved. The investigators will examine 2 groups of 30 patients each with clean hand lacerations involving tendons. One group will be treated with prophylactic antibiotic and the other wont be treated, randomly. The investigators assume that the rate of wound infection wont be different between the 2 groups.

02

Conditions studied

  • Hand Laceration
  • Tendon Involved
  • Clean Laceration
  • No Bone Involved

Browse trials for

Keywords

  • Lacerations
  • Tendons
  • Antobiotic
03

In context

Lacerations

133 studies on the registry are indexed under Lacerations; 29 are open to participants now.

This study's enrollment of 24 is below the median of 79 across 106 interventional studies indexed under Lacerations.

Browse Lacerations studies →

Lead sponsor

HaEmek Medical Center, Israel is the lead sponsor of 228 studies on the registry; 12 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
13 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Hand laceration
  • Tendon involeved
  • Clean laceration
  • No bone involved

Exclusion criteria

Exclusion Criteria:

  • Pregnant
  • Children
  • Immunocompremised patients
  • "Dirty" lacerations
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
24 participants (actual)

Study arms

  • Experimental
    with antibiotic and without antibiotic

    Drug: Antibiotic-Cefamezin

Interventions

  • DrugAntibiotic-Cefamezin

    Also known as: Ceforal, Keflex

06

What researchers measure

Primary outcomes

  1. rate of wound infections

    signs of wound/tissue infection, levels of WBC, ESR, CRP

    Time frame: 2 years

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 17, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01899781
Lead sponsor
HaEmek Medical Center, Israel
Responsible party
Sponsor
First posted
Jul 15, 2013
Start date
Aug 2013
Primary completion
Jan 2015
Completion
Nov 2015
Last update
Feb 17, 2020

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2020. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion