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Recurrence clinical trials

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NCT ID: NCT04178642 Withdrawn - Clinical trials for Hepatocellular Carcinoma

The Impact on Hepatic Recurrence After Adjuvant Chemotherapy With Intraarterial Infusion of Idarubicin-Lipiodol

LIDA-ADJ
Start date: September 22, 2020
Phase: Phase 2
Study type: Interventional

The aim of this study is to test whether the realization of 3 courses of intra-arterial chemotherapy of idarubicin-lipiodol without embolization, administered non-selectively in the hepatic artery, following the percutaneous tumour ablation of a hepatocellular carcinoma, could constitute an effective adjuvant treatment to reduce the rates of local and intrahepatic distant recurrence and thus improve the survival without hepatic progression.

NCT ID: NCT04149145 Withdrawn - Clinical trials for Ovarian Cancer Recurrent

Trial of M4344 and Niraparib in Patients With Poly (ADP-ribose) Polymerase (PARP) Resistant Recurrent Ovarian Cancer

PARP
Start date: May 2023
Phase: Phase 1
Study type: Interventional

The purpose of this study is to find out if a new drug, M4344, is safe and has beneficial effects when given in combination with the PARP inhibitor, Niraparib, in women with recurrent ovarian cancer that has progressed while on a PARP inhibitor.

NCT ID: NCT04029038 Withdrawn - Clinical trials for Refractory Chronic Lymphocytic Leukemia

Modified Immune Cells (CD19-CD22 CAR T Cells) in Treating Patients With Recurrent or Refractory CD19 Positive, CD22 Positive Leukemia or Lymphoma

Start date: May 15, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

This phase I/II trial studies the side effects and best dose of modified immune cells called CD19-CD22 chimeric antigen receptor (CAR) T cells in treating patients with CD19 positive(+), CD22+ B-acute lymphoblastic leukemia, chronic lymphocytic leukemia, or non-Hodgkin's lymphoma that has come back (recurrent) or does not respond to treatment (refractory). T-cells are collected from the patient and genetic materials called "chimeric antigen receptors (CAR)" are transferred to the collected T-cells. The CAR T-cells are then infused back to the patient's body. Giving CD19- CD22 CAR T cells after chemotherapy may help to control the disease.

NCT ID: NCT03955068 Withdrawn - Ketogenic Diet Clinical Trials

Strict Classic Ketogenic Diet as a Therapy for Recurrent or Progressive and Refractory Brain Tumors in Children

Start date: July 2024
Phase: N/A
Study type: Interventional

This is a pilot study to test the feasibility of implementing a strict classic ketogenic diet among a population of children with recurrent or progressive and refractory brain tumors. Eligible participants will be admitted to the neurosciences floor for 5 days to begin the ketogenic diet either orally, by gastrostomy tube or via nasogastric tube. During the inpatient stay, they will be extensively educated on the diet restrictions and rules. Participants will then continue on the diet at home returning about 17 times over the next 12 months. Daily logs will be kept tracking diet changes, bowel movements and urine ketones. Blood will be collected during the inpatient stay and at all visits for both standard clinical care and research testing.

NCT ID: NCT03845322 Withdrawn - Clinical trials for Hematoma, Subdural, Chronic

Curcumin/Turmeric as a Treatment for Patients With Subdural Hematomas Recurrence

CACTIS
Start date: December 18, 2018
Phase: Early Phase 1
Study type: Interventional

Our long-term objective is to evaluate the efficacy of curcumin (CC) in preventing a recurrence of chronic subdural hematoma (cSDH) following surgical evacuation. Recurrence is defined as an increase in total hematoma volume on the operated side compared to a post-operative day one CT scan with persistent or recurrent neurological symptoms. The investigators propose this pilot study to assess feasibility and obtain preliminary benefit assessment of the proposed therapeutic approach. Objective 1: To determine if the use of CC treatment reduces the total hematoma cavity volume over a 6-month interval, compared to a post-subdural drain removal CT scan. This evaluation is expected to offer sufficient evidence for a larger definitive trial. Objective 2: Study the effect of CC on interleukin-8 (IL-8)-induced disruption of endothelial permeability in vitro using human vascular endothelial cells. Central hypothesis: CC treatment prevents the re-accumulation of cSDH, which may occur by inhibition of IL-8 and allowing resolution of the total hematoma cavity volume over six months.

NCT ID: NCT03787251 Withdrawn - Clinical trials for Esophageal Neoplasms

A Study of Second-line Treatment of Postoperative Recurrence and Metastasis of Esophageal Cancer Treated With Apatinib

Start date: January 1, 2019
Phase: Phase 2
Study type: Interventional

A study of second-line treatment of postoperative recurrence and metastasis of esophageal squamous cell carcinoma after chemotherapy with apatinib mesylate

NCT ID: NCT03670134 Withdrawn - Barrett Esophagus Clinical Trials

Predict Recurrence of Barrett's Esophagus After Complete Eradication of Intestinal Metaplasia

Start date: August 6, 2018
Phase: N/A
Study type: Interventional

Researchers are trying to see if the Nvision® Imaging System (VLE) can accurately determine the risk of recurrent Barrett's esophagus in patients with Barrett's esophagus which have been clear of disease.

NCT ID: NCT03634683 Withdrawn - Clinical trials for Recurrent Hepatocellular Carcinoma

A Study of LioCyx in Patient With Recurrent HBV-related HCC Post Liver Transplantation

Start date: August 2018
Phase: Phase 1/Phase 2
Study type: Interventional

Hepatocellular carcinoma (HCC) represent approximately 70-85% of liver cancer, in which Hepatitis B virus (HBV) is the major etiologic agent accounting for at least 80% of HCC in Asian countries. Overall, transplantation remains the best option however, HCC recurrence rate is high among liver transplant patients. While there are limited treatment measures for HBV-related HCC recurrences, the study hypothesized that LioCyx is capable of lysing target liver cells expressing the HBV cognate antigens and provide clinical benefit to patients with HBV-related HCC.

NCT ID: NCT03626376 Withdrawn - Clinical trials for Herpes Simplex Virus Keratitis

Topical Corticosteroid Use in Addition to Oral Antivirals for Prevention of Recurrence of Herpes Simplex Virus (HSV) Keratitis

Start date: December 10, 2019
Phase: Phase 4
Study type: Interventional

This is a prospective, randomized clinical trial looking to determine the role of prophylactic treatment with topical corticosteroids in preventing recurrences in patients with a history of infectious epithelial keratitis, stromal keratitis,endotheliitis, or iridocyclitis. Patients will be enrolled to one of two treatment arms: Control arm: oral acyclovir 400 mg BID OR valacyclovir 500 mg daily or Study arm: oral acyclovir 400 mg BID OR valacyclovir 500 mg qdaily + topical corticosteroid eye drops.

NCT ID: NCT03524638 Withdrawn - Colorectal Cancer Clinical Trials

Visbiome Effect on Colorectal Anastomosis and Local Recurrence

Start date: April 13, 2018
Phase: N/A
Study type: Interventional

Determine whether the administration of Visbiome after colorectal surgery has any effect on anastomotic leak and local recurrence