Lumbar Stabilization Surgery

2

Review clinical trials related to Lumbar Stabilization Surgery. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Effect of Prone Position on Continuous Noninvasive Hemoglobin Measurement

This prospective observational study aims to evaluate whether the prone position affects the agreement between noninvasive hemoglobin (SpHb) measurements and laboratory hemoglobin values in patients undergoing lumbar stabilization surgery under general anesthesia. SpHb provides continuous, noninvasive monitoring of hemoglobin using multi-wavelength pulse CO-oximetry. However, its accuracy may be affected by changes in peripheral perfusion, hemodynamic status, and patient position. The prone position used during spine surgery may alter cardiovascular function and peripheral perfusion and may therefore influence SpHb measurements. In this study, SpHb values obtained in the supine and prone positions will be compared with simultaneously obtained laboratory hemoglobin values. The study will also evaluate the ability of SpHb to follow changes in hemoglobin during surgery. The results may help clarify the clinical usefulness of continuous noninvasive hemoglobin monitoring during surgery performed in the prone position.

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research HospitalUpdated: Sep 16, 2026Locations: 1
Eligibility criteria

Age 18 years or older [+3]

Refusal to participate in the study [+3]

Status: Not yet recruiting

ESP Block Vs. QIPB for Lumbar Stabilization Surgery

This randomized clinical trial aims to evaluate and compare the analgesic efficacy and functional outcomes of the quadro-iliac plane block (QIPB) and the erector spinae plane block (ESPB) in patients undergoing lumbar stabilization surgery. The primary outcome is the Numeric Rating Scale (NRS) within the first 48 hours after surgery. Secondary outcomes include postoperative total opioid consumption, incidence of quadriceps motor block, time to first ambulation, block performance time, falls, length of hospital stay, block-related complications (hematoma, local anesthetic systemic complications, vascular puncture, and infection), patient satisfaction assessed using a Likert scale, and incidence of postoperative nausea and vomiting.

Participants needed: 60
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Antalya City HospitalUpdated: Aug 27, 2026
Eligibility criteria

Age between 18 and 80 years [+5]

Refusal to participate [+13]