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Dye test may reveal hidden blood flow after filler mishaps

NCT ID NCT07581652

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looked at whether indocyanine green angiography (ICGA), a dye-based imaging test, can help doctors assess blood flow in the face after a rare but serious complication from hyaluronic acid filler injections. Researchers reviewed medical records and images from 19 patients who had already received treatment for a blocked artery. The goal was to see if ICGA could provide real-time information on tissue perfusion and help predict recovery.

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 angiography (ICGA)
What this could lead to
If successful, this could show that ICGA is a useful tool for doctors to quickly see how well blood flow is returning after treatment for a blocked artery from filler injections.
What could go wrong
This is a very small, retrospective study (19 people) that only looks back at existing data. It cannot prove that ICGA improves patient outcomes, only that it might be helpful for assessment.

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

19 people

The number who actually took part.

Started

Jul 2025

Finished

Mar 2026

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.

Who is studied

The study population consists of consecutive patients treated at the Center for Wound Repair and Tissue Regeneration, Plastic Surgery Hospital, Chinese Academy of Medical Sciences, for facial vascular embolism following hyaluronic acid injection between July 2025 and March 2026. Participants will be identified retrospectively from existing medical records, indocyanine green angiography imaging data, treatment records, and follow-up documentation generated during routine clinical care.

Ages

18 years and older

Sex

Anyone

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: * History of facial hyaluronic acid injection. * Clinical diagnosis of facial vascular embolism after hyaluronic acid injection, with symptoms or signs such as pain, skin color change, livedo-like discoloration, delayed capillary refill, or tissue ischemia. * Received initial rescue treatment at the study center. * Had indocyanine green angiography imaging performed before and immediately after initial rescue treatment as part of routine clinical care. * Had sufficient medical records and follow-up information available to assess subsequent treatment and tissue outcomes. Exclusion Criteria: * Incomplete indocyanine green angiography imaging data. * Insufficient medical records or follow-up information to assess the main study outcomes. * Missing key clinical information needed for study analysis. * Duplicate records or records with concerns about data reliability. * The patient or legal representative explicitly objected to the use of historical clinical data for this study, if applicable under local ethics requirements.

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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

  • Plastic Surgery Hospital, Chinese Academy of Medical Sciences

    Beijing, Beijing Municipality, 100144, China