Clinical trial Recruiting at 1 site Observational Ages 18 and up

Prone Position and Noninvasive Hemoglobin Monitoring in Spine Surgery

Official title: Does the Prone Position Affect Continuous Noninvasive Hemoglobin Measurement?

Run by Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital · NCT07823569 · Data updated 2026-11-12

This study tests whether being in the prone position changes how closely a finger-based hemoglobin monitor (SpHb) matches lab hemoglobin in adults undergoing lumbar stabilization surgery under anesthesia.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment80 (estimated)
SponsorSehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital
Academic / other
Locations1 site (Istanbul, Istanbul)
StatusRecruiting
StartedSeptember 11, 2026
Main results expectedDecember 31, 2026
Study endsDecember 31, 2026
Registry record updatedSeptember 16, 2026
Trial IDNCT07823569 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18 years or older with ASA I–III scheduled for lumbar stabilization surgery under general anesthesia who consent to participate.

Probably not a fit

Patients with ASA IV–V, peripheral arterial disease, or hemoglobin <10 g/dL may not benefit from SpHb monitoring in this study.

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

What this trial studies

This prospective, single-center observational study will compare SpHb measurements taken in supine and prone positions with laboratory hemoglobin values obtained from blood gas analyses during lumbar stabilization surgery. It will also assess whether SpHb can track intraoperative changes in hemoglobin. Eligible participants are adults (18+) with ASA I–III undergoing the procedure and able to consent. Data collected include intraoperative hemodynamics, blood loss, transfusions, ICU stay, and total hospital stay to evaluate the performance and potential clinical utility of continuous noninvasive hemoglobin monitoring in the prone position.

Why it matters

Potential benefit: If successful, the study could validate SpHb as a reliable continuous monitor during spine surgery, potentially aiding real-time decision-making about blood management.

How similar studies have gone: Prior research suggests SpHb can track hemoglobin trends but accuracy may be influenced by position and perfusion; this study adds prospective data in the prone setting.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 18 years or older
* American Society of Anesthesiologists (ASA) physical status I-III
* Scheduled to undergo lumbar stabilization surgery under general anesthesia
* Provision of written informed consent for participation in the study

Exclusion Criteria:

* Refusal to participate in the study
* ASA physical status IV-V
* Hemoglobin level \<10 g/dL
* Presence of peripheral arterial disease

Where it's running

  • Sancaktepe Sehit Prof. Dr. Ilhan Varank Training and Research Hospital
    Istanbul, Istanbul, Turkey (Türkiye)
    Recruiting

Study contacts

  • Principal investigator: Altuncu — Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital
  • Study coordinator: Şule Altuncu, MD
  • Email: sancaktepeetikkurul@gmail.com
  • Phone: 02166063300

Similar studies

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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.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.