Effects of Intensive Glycemic Control in the Postoperative Period of Neurosurgical Patients on the Incidence of Surgical Site Infection

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Sao Paulo

About this trial

Surgical site infections (SSIs) are frequent complications in neurosurgical patients, often worsened by perioperative hyperglycemia. This randomized, controlled trial will compare intensive glycemic control (continuous insulin infusion, 140-180 mg/dL) with standard care (subcutaneous insulin, 81-180 mg/dL) in 544 patients. The primary outcome is SSI occurrence within 90 days post-surgery. Results aim to guide optimal glycemic management for SSI prevention in neurosurgery.

Eligibility criteria

Qualifiers

Adults aged ≥18 years

Patients undergoing elective cranial neurosurgical procedures classified as clean surgeries

Disqualifiers

Patients who underwent any surgical or neurosurgical procedure within 30 days prior to enrollment

Presence of active infection at any site

Patients undergoing emergency or urgent neurosurgical procedures

Patients with trauma and exposed brain tissue

Trial design

Treatments tested in this trial

  • Intensive glycemic control
  • Hypokalemia Prevention Protocol During IV Insulin Therapy
  • Glucose-Supported Intravenous Insulin Infusion Protocol

Treatment groups

572 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators