Comparing iodine and chlorhexidine solutions for reducing infections in spinal surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness of povidone-iodine and chlorhexidine gluconate solutions in reducing bacterial contamination during spinal surgery. It aims to determine which antiseptic solution is more effective for intraoperative wound irrigation and to assess any potential side effects associated with their use. Patients diagnosed with lumbar spinal stenosis scheduled for open spinal decompression and fusion surgery will be included in the study. The research will involve intraoperative sampling to measure bacterial load before closing the surgical wounds.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients who were diagnosed with lumbar spinal stenosis need to undergo posterior lumbar decompression with fusion surgery.

Exclusion Criteria:

* People who are allergic to disinfectants (Providine or CHG)
* The surgical site has been operated before.
* Patients under active infection status.

Where it's running

• National Cheng Kung University Hospital
  Tainan, Taiwan, Taiwan Recruiting

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.