Clinical trials

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

Condition / disease
Location
Status: Recruiting

Comparison of Oral Administration of a JAK Inhibitor in Rheumatoid Arthritis

The aim of this study is to offer patients two treatment options: morning or evening administration of a JAK inhibitor prescribed within the framework of its marketing authorization, according to the EULAR response. The objective is to determine whether evening administration in our patients with rheumatoid arthritis provides greater efficacy than morning administration in our patients taking JAK inhibitors once daily.

Participants needed: 90
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Centre Hospitalier Princesse GraceUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Patient aged over 18 years [+3]

No contraindication to a bDMARD [+8]

Status: Recruiting

Pain Assessment During Rapid Sequence Induction

Rapid sequence induction (RSI) is a standard anesthesia technique used in patients at risk of aspiration. Although tracheal intubation following RSI is a frequent and painful procedure, no study has yet evaluated nociception using the Analgesia Nociception Index (ANI) during this procedure. This monocentric prospective observational study aims to describe the impact of RSI on pain measured by ANI, and to explore early complications (desaturation, hypotension, regurgitation) and factors associated with pain and complications. 150 patients undergoing RSI in the visceral surgery operating room at CHPG Monaco will be analyzed.

Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Centre Hospitalier Princesse GraceUpdated: May 27, 2026Locations: 1
Eligibility criteria

Age >= 18 years [+2]

Patient with atrial fibrillation at the time of intubation following rapid seque... [+1]

Status: Recruiting

Glial Fibrillary Acidic Protein (GFAP) and Ubiquitin Carboxy-terminal Hydrolase L1 (UCH-L1) to Exclude Lesions Linked to Significant Traumatic Brain Injuries

The goal of this observational study is to evaluate the performance of UCH-L1 and GFAP combined in patients with a mild traumatic brain injury. The main question : • Does the combination of UCH-L1 and GFAP can exclude brain injuries detected with CT scan in the first twelve hours after a mild traumatic brain injury? Participants will do the exams planed in routine care and : * during the expected blood sampling an additional blood sample will be done, * seven days after the discharge a call will be done by the investigator.

Participants needed: 1,500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Centre Hospitalier Princesse GraceUpdated: Feb 19, 2025Locations: 15
Eligibility criteria

Traumatic brain injury defined by [+10]

Person not affiliated or not benefiting from a health insurance scheme. [+11]

Status: Recruiting

Observational Study on the Treatment of Trigeminal Neuralgia by Radiosurgery

This study aims to evaluate the outcome of patient treated by radiosurgery on LINAC with high dose rate for classical trigeminal neuralgia

Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Centre Hospitalier Princesse GraceUpdated: Feb 19, 2025Locations: 1Duration: 10 Years
Eligibility criteria

Classical trigeminal neuralgia according the International Classification of Hea... [+2]

Patients suffering from secondary Trigeminal neuralgia (tumour in the cerebellop... [+1]