Clinical trials

4

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Radiographic Head and Neck Positional Changes in Response to Usage of Low-powered Prismatic Lenses

This study aims to investigate the short-term modifications in head and neck positioning by usage of low-powered prismatic lenses in patients with Postural Deficiency Syndrome (PDS). A matched pair observation study was designed. Evaluation is carried out using low dose biplanar radiography before treatment and 15 minutes after lenses application.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Lisbon Academic Medical Center - Centro Académico de Medicina de LisboaUpdated: Apr 16, 2026Locations: 1
Eligibility criteria

Two or more cardinal signs of Postural Deficiency Syndrome [+2]

Vision under 8/10, strabismus or nistagmus; [+4]

Status: Recruiting

UP STUDY - Decipher Persistent Critical Illness Through in Deep Clinical Phenotyping.

Persistent Critical Illness (PCI) is a condition that affects some patients who remain in the Intensive Care Unit (ICU) for a long time, usually more than 10-14 days. It is estimated to occur in 5-20% of critically ill patients. A recent Portuguese study found that more than 14% of ICU patients stayed longer than 14 days. PCI is often associated with ongoing need for life support, such as mechanical ventilation or medications to maintain blood pressure. However, patients may also experience severe muscle weakness, repeated infections, or other complications, which makes this group very diverse. One of the main risk factors for prolonged ICU stay is sepsis, a severe infection that affects the whole body. Other factors-such as prior health conditions, use of corticosteroids, sedation practices, early versus late mobilization, fluid and antibiotic management, and delirium treatment-may also influence the development and course of PCI. This study aims to identify different clinical patterns ("clusters") among critically ill patients who remain in the ICU for more than 10 days. Patients will be followed until hospital discharge, and up to one year if data are available. Understanding these different patterns will help develop more personalized and effective care strategies for each patient profile. The study is a multicenter retrospective cohort including adult patients (≥18 years) admitted to participating ICUs for more than 5 days between 2021 and 2023. Data collected will include demographic, clinical, and laboratory information, details of organ support (such as mechanical ventilation or vasopressors), medications, nutrition, and rehabilitation practices. Statistical and machine learning methods will be used to identify groups of patients with similar clinical trajectories and to assess how these groups are related to outcomes such as survival, recovery of organ function, or long-term disability. Expected results are the identification of distinct clinical clusters of PCI that combine clinical and laboratory data, and the development of tailored management strategies to improve recovery and outcomes for patients with PCI.

Participants needed: 7,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Lisbon Academic Medical Center - Centro Académico de Medicina de LisboaUpdated: Apr 13, 2026Locations: 7
Eligibility criteria

Adult patients aged 18 years or older; [+1]

Patients with an ICU stay < 5 days; [+2]

Status: Recruiting

Cardiac Remodelling Following Endovascular Repair of the Aorta

To assess the effects of endovascular aortic repair on cardiac morphology and function

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Lisbon Academic Medical Center - Centro Académico de Medicina de LisboaUpdated: Feb 17, 2026Locations: 2
Eligibility criteria

Heart failure with an ejection fraction <35 vs 50% or New York Heart Association... [+10]

Status: Recruiting

The Triad of Nutrition, Intestinal Microbiota and Rheumatoid Arthritis (TASTY)

The main goal of this trial is to investigate whether a dietary intervention based on a typical Mediterranean Diet enriched with fermented foods (MedDiet+) can impact gut microbiota and RA-related outcomes.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Lisbon Academic Medical Center - Centro Académico de Medicina de LisboaUpdated: Jan 6, 2025Locations: 2
Eligibility criteria

RA patients (ACR/EULAR2010 criteria) [+6]

Prednisolone dose ≥ 7.5 mg/day [+11]