P=N/A, N=300, Not yet recruiting, Beijing Shijitan Hospital, Capital Medical University, Beijing; Beijing Shijitan Hospital, Capital Medical University
Additionally, the cTnI level in the levosimendan group was significantly lower than that in the dobutamine group (1.01±0.54 ng/ml vs. 1.40±0.63 ng/ml, P=0.042), and LVEF was significantly higher in the levosimendan group (50.60±6.11% vs. 46.90±4.95%, P=0.042). These findings suggest that levosimendan may reduce plasma IL-6 levels, alleviate myocardial injury, and improve myocardial contractility in patients with septic cardiomyopathy compared to dobutamine.
The findings advocate that cilostazol exerts neuroprotective effects against LPS-induced hippocampal injury by modulating the AKT/GSK3β/CREB pathway and curbing neuroinflammation. Cilostazol may hold promise as a therapeutic agent for neuroinflammatory conditions associated with neurodegenerative diseases.
P3, N=82, Terminated, Centre Hospitalier Universitaire Dijon | N=210 --> 82 | Trial completion date: Feb 2024 --> Oct 2023 | Recruiting --> Terminated | Trial primary completion date: Feb 2023 --> Oct 2023; There was insufficient funding to continue the study in good conditions.
2 months ago
Enrollment change • Trial completion date • Trial termination • Trial primary completion date
P3, N=900, Recruiting, Kafrelsheikh University | Trial completion date: Mar 2024 --> Dec 2024 | Initiation date: Dec 2021 --> Dec 2023 | Trial primary completion date: Jan 2024 --> Dec 2024
3 months ago
Trial completion date • Trial initiation date • Trial primary completion date
P2/3, N=70, Active, not recruiting, Ain Shams University | Recruiting --> Active, not recruiting | Trial completion date: Oct 2023 --> Oct 2024 | Trial primary completion date: Oct 2023 --> Oct 2024
3 months ago
Enrollment closed • Trial completion date • Trial primary completion date
P2, N=120, Recruiting, VA Office of Research and Development | Trial completion date: Dec 2024 --> Dec 2025 | Trial primary completion date: Jun 2024 --> Jun 2025
4 months ago
Trial completion date • Trial primary completion date
These findings suggest that OPB-171775, with its significant efficacy, could potentially serve as a novel and effective treatment option for advanced GISTs, particularly those resistant to TKIs.
The above findings suggest that ALP plus CIL is effective for patients with LEASO receiving evidence-based care. It can significantly improve arteriosclerosis indexes and hemorheological parameters while inhibiting serum inflammatory responses, with some certain safety.