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New sensor may replace needles for blood monitoring during spine surgery

NCT ID NCT07054411

Knowledge-focused Sponsor: Erhan Ozyurt Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at 53 scoliosis surgery patients to see if a non-invasive finger sensor (Radical-7 Pulse CO-Oximeter) could accurately measure hemoglobin levels compared to standard blood draws. Researchers recorded hemoglobin readings from the sensor and from lab tests every hour during surgery. The goal was to see if the sensor could reliably track blood loss without needing frequent blood samples.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

53 people

The number who actually took part.

Started

Jul 2025

Finished

Mar 2026

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Patients who apply to our hospital's orthopedic clinics to undergo elective scoliosis surgery.

Ages

5 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Preoperative hemoglobin ≥ 9 g/dL * ASA I - III Exclusion Criteria: * Patients with hematological disease, * Uncorrected preoperative anemia (preoperative hemoglobin \< 9 g/dL)

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Conditions

The condition(s) this trial relates to.

scoliosis

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Scoliosis patients

Contacts and locations

Locations

  • University of Health Sciences Antalya Training and Research Hospital

    Antalya, 07000, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.