Glowing dye could make spine surgery safer
NCT ID NCT05808140
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a green dye called indocyanine green (ICG) can help surgeons see and protect nerves during spine surgery for a slipped disc. Forty patients were split into groups: some got the dye and a special camera, others had standard surgery. The goal was to see if the dye makes finding nerves faster and safer, potentially reducing nerve damage that can cause numbness or weakness.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Indocyanine Green (ICG)
- What this could lead to
- If it works, this could make spine surgery safer by helping surgeons avoid damaging nerves, reducing the risk of numbness or weakness after surgery.
- What could go wrong
- This is an early-phase trial with only 40 people, so results may not apply to everyone. The dye might not work well in all patients, and there is a small risk of allergic reactions.
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.
- Phase
-
Phase 1/2
Runs two stages together: safety and dose first, then whether the treatment works.
- Participants
-
40 people
The number who actually took part.
- Started
-
Apr 2023
- Finished
-
Dec 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
20 to 60 years
- 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 Hide 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: * Patients diagnosed with lumbar disc herniation based on symptoms and Imaging examination * Patients undergo endoscopy spinal surgery for nerve root decompression * Patients have no clear contraindications to surgery, and has the ability to understand and act and has informed consent, and can participate in all study follow-up voluntarily and signe a written informed consent form. Exclusion Criteria: * The patients have thyroid related diseases, including autonomous nodules * Patients are allergic to iodine or shellfish * Patients have ankylosing spondylitis, lumbar instability or bony spinal stenosis * Patients have diabetes, vascular related diseases, or abnormal liver and kidney function * Difficulty in tolerating anaesthesia * Pregnant or lactating women * Patients are unable to communicate or do not follow directions * The investigators consider the patient unsuitable to participate in this study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Department of Spine Surgery and Musculoskeletal Tumor, Zhongnan Hospital of Wuhan University
Wuhan, Hubei, 430062, China
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