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NOT YET RECRUITING
NCT07467798
NA

A Proof-of-concept Study of Ultrasound Stimulation of the Neck to Enhance Anti-shock Efficacy

Sponsor: Tao Liu

View on ClinicalTrials.gov

Summary

The objective of this clinical study is to evaluate the initial efficacy and safety of LIPUS as an adjunct to standard therapy in patients with traumatic hypovolemic shock. The investigators will invite patients to participate in a proof-of-concept study investigating the efficacy of neck ultrasound stimulation to enhance anti-shock treatment, involving brief exposure to low-intensity pulsed ultrasound. This study examines whether LIPUS can enhance blood pressure in patients with traumatic hypotension, improve the efficacy of antihypotensive treatment, and reduce the dosage and duration of vasoactive drugs during active pharmacological therapy. By applying LIPUS as an adjunct to conventional treatment in clinical cases of traumatic hypotension, we aim to determine the clinical value of LIPUS and establish a theoretical foundation for developing innovative new therapies for hypotension.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2026-03

Completion Date

2027-10

Last Updated

2026-03-12

Healthy Volunteers

No

Conditions

Interventions

DEVICE

Low-intensity pulsed ultrasound

During periods of stable blood pressure, administer cervical ultrasound stimulation (3-minute stimulation followed by a 2-minute interval, repeated cyclically; total stimulation duration not exceeding 60 minutes).