Prospective Study of High-penetration Super-resolution Transcranial Ultrasound for Early Identification of Postoperative Intracranial Metallic Targets After Aneurysm Clipping

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-85
SponsorChinese PLA General Hospital

About this trial

To evaluate the patient-level early diagnostic performance of high-penetration super-resolution transcranial ultrasound for identifying intracranial metallic targets, and to further assess clip-level detection, localization, agreement, and its complementary value to routine postoperative imaging.This study does not alter routine clinical treatment. All participants will undergo standardized high-penetration super-resolution transcranial ultrasound within 3 hours after surgery. Postoperative CT is mandatory for all participants; CTA or other routine postoperative imaging will be obtained only when clinically indicated.

Eligibility criteria

Qualifiers

Age 18-85 years;

Positive group: patients undergoing intracranial aneurysm clipping with implanted metallic clips; negative control group: postoperative craniotomy patients without implanted clips;

Ability to complete transcranial ultrasound within 3 hours after surgery;

Availability of postoperative CT;

Disqualifiers

Inability to complete standardized transcranial ultrasound;

Missing postoperative CT;

Inability to establish the composite reference standard;

Presence of non-study-related metallic materials that may substantially interfere with target identification;

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

78 Participants
are grouped into 2 trial groups

Locations

This trial has no locations

Sponsors and collaborators