Mild Therapeutic Hypothermia

2

Review clinical trials related to Mild Therapeutic Hypothermia. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Evaluation of MTH in PCI Under VA-ECMO for AMICS

This study is a randomized controlled trial conducted at Beijing Anzhen Hospital, Capital Medical University. The primary objective is to assess the efficacy of mild therapeutic hypothermia in reducing infarct size and improving cardiac function in patients receiving percutaneous coronary intervention under venous-arterial extracorporeal membrane oxygenation for acute myocardial infarction complicated with cardiogenic shock. Secondary objectives include evaluating the safety of mild therapeutic hypothermia and its impact on venous-arterial extracorporeal membrane oxygenation weaning success and short-term survival.

Participants needed: 44
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Beijing Anzhen HospitalUpdated: Sep 22, 2025
Eligibility criteria

Patients diagnosed with acute myocardial infarction complicated by cardiogenic s... [+2]

Cardiogenic shock lasting more than 12 hours or a history of chronic congestive... [+9]

Status: Recruiting

Non-Invasive System to Deliver Therapeutic Hypothermia for Protection Against Noise-Induced Hearing Loss

The goal of this interventional clinical study is to investigate the use of mild therapeutic hypothermia devices for preservation of sensory structures in the cochlea after noise exposure. The main aims of the study are: 1. To test the safety and best duration for use for a new hypothermia device. 2. To determine if the hypothermia device helps decrease noise-induced hearing loss in a group of firefighters. Participants will wear the mild therapeutic hypothermia therapy devices immediately after a fire service shift serially over a year. Researchers will compare results from those receiving the therapy to those from a control group (individuals receiving no therapy and a sham therapy).

Participants needed: 116
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: Restorear Devices LLCUpdated: Apr 2, 2025Locations: 1
Eligibility criteria

Adults aged 18-55 years old at the time of signing the consent form [+1]

Abnormal tympanometric findings [+7]