This study is currently not recruiting participants.

Development of an OR Bundle

Observational Study on Procedures and Surgical Site Infections

Not Recruiting
100 years or below
All
Phase N/A
1 Location

Brief description of study.

The study will be an observational study done by the neurosurgical team on their shunt procedures. The data elements will be collected and maintained under patient medical record number so any surgical site infection that appears within 1 year of the pro

Detailed description of study

The study will be an observational study done by the neurosurgical team on their shunt procedures. The data elements will be collected and maintained under patient medical record number so any surgical site infection that appears within 1 year of the pro

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Surgery
  • Age: 100 years or below
  • Gender: All

This study investigates the outcomes of shunt procedures conducted by a neurosurgical team. A shunt is a tube that is used to drain fluid from the brain to another part of the body. The purpose of this study is to observe any surgical site infections that may occur within one year after the procedure.

Participants' medical records will be used to collect data on surgical site infections. This data will be maintained under the patient's medical record number to ensure accuracy and confidentiality.

  • Who can participate: Participants must meet general eligibility criteria, including being adults aged 18 and over who have undergone shunt procedures.
  • Study details: Participants will not need to take any specific actions as this is an observational study using existing medical records.
  • Study Timelines: The study will last 1 year.
Updated on 19 Feb 2024. Study ID: 1210009802

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