Survival Rate

2

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

Condition / disease
Location
Status: Not yet recruiting

Clinical Outcomes of Early Kasai Surgery With Umbilical Cord MSCs in Biliary Atresia

The goal of this clinical trial with historical control is to evaluate whether umbilical cord-derived mesenchymal stem cell (UC-MSC) therapy can improve clinical outcomes in infants with biliary atresia undergoing Kasai surgery before 90 days of age. The main questions it aims to answer are: Does UC-MSC therapy improve liver function parameters (bilirubin, albumin, liver enzymes, coagulation profile)? Does UC-MSC therapy reduce complications such as anemia, ascites, jaundice, and improve PELD scores? Does UC-MSC therapy improve overall survival compared to standard Kasai surgery alone? Researchers will compare the group receiving UC-MSC in 2025-2027 with a historical control group of patients who previously underwent Kasai surgery without UC-MSC therapy. Participants will: Undergo preoperative evaluation, including laboratory and imaging tests. Receive Kasai surgery combined with intraoperative trans-portal vein injection of 20 million UC-MSCs. Be monitored postoperatively through serial laboratory tests, imaging (Fibroscan), and clinical assessments at scheduled intervals. Be followed up for potential serious adverse events and survival outcomes.

Participants needed: 14
Trial details
Phase: Phase 1Age: 0-90Biological sex: AllType: InterventionalSponsor: Universitas DiponegoroUpdated: Jun 8, 2025Locations: 1
Eligibility criteria

Infants diagnosed with biliary atresia confirmed by intraoperative findings. [+2]

Infants with severe malnutrition. [+2]

Status: Not yet recruiting

Effect of HIPEC After Radical Surgery on Long-term Survival for Locally Advanced Gastric Cancer

The study focuses on patients with locally advanced gastric adenocarcinoma (cT3N+M0 and cT4aN+/-M0), assessing the feasibility, surgical safety, and oncological benefit of prophylactic HIPEC treatment following laparoscopic D2 radical surgery.

Participants needed: 302
Trial details
Phase: Early Phase 1Age: 18-70Biological sex: AllType: InterventionalSponsor: The First Hospital of Jilin UniversityUpdated: Jul 31, 2024
Eligibility criteria

Age >18 and ≤70 years; [+6]

Other cancers within the past 5 years; [+7]