Investigation Into the Safety and Efficacy of ICG-Labeled Fluorescence Imaging Technology in Guiding the Resection of Bone and Soft Tissue Tumors

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorGuangdong Provincial People's Hospital

About this trial

Investigate the application protocol, feasibility, and efficacy of indocyanine green (ICG)-assisted near-infrared (NIR) fluorescence-guided resection in bone and soft tissue tumors. Assess the incidence of adverse events and evaluate the safety of the protocol.

Eligibility criteria

Qualifiers

Histologically confirmed diagnosis of bone and soft tissue tumors (according to the WHO Classification of Tumours of Soft Tissue and Bone, 4th Edition).

Medically fit to undergo surgical treatment based on preoperative evaluation.

Absence of cardiovascular, anesthesia-related, or other surgical contraindications.

Disqualifiers

Presence of severe or chronic kidney, liver, or pulmonary diseases.

Autonomous thyroid nodules or allergy to iodine/shellfish.

Deemed unable to tolerate surgery based on preoperative evaluation.

Trial design

Treatments tested in this trial

  • Indocyanine green (ICG)

Treatment groups

40 Participants
are divided into 1 treatment group