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Recurrence clinical trials

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NCT ID: NCT04239742 Recruiting - Clinical trials for Prostate Cancer Recurrent

F18-PSMA-1007 PET for Early Biochemical Recurrence of Prostate Cancer

PROPER-ABX
Start date: January 2, 2020
Phase: N/A
Study type: Interventional

18F-PSMA-1007 is a new radiopharmaceutical for the detection of prostate cancer with potential benefits over the registered 18F-Fluciclovine (Axumin). The main potential benefit is the higher detection rate of PSMA compared to Fluciclovin in the low PSA range. It may therefore be more sensitive in detecting local disease in case of biochemical recurrens. The investigators aim to compare the detection efficacy of 18F-PSMA-1007 to 18F-Fluciclovin in prostate cancer patients with biochemical recurrence (PSA levels 0.2-5 ng/ml).

NCT ID: NCT04239365 Completed - Colorectal Cancer Clinical Trials

Follow-up Protocol of Colorectal Endoscopic Mucosal Resection Scars

Start date: January 31, 2020
Phase: N/A
Study type: Interventional

Nowadays endoscopic mucosal resection (EMR) is the gold standard for the removal of large laterally spreading and sessile colorectal lesions ≥ 20 mm. However, recurrence rate after successful EMR (defined by the absence of neoplastic tissue at the completion of the procedure after careful inspection of the post-EMR mucosal defect and margin) is about 15-20%. Consequently, current guidelines recommend a surveillance colonoscopy between 4 and 6 months after resection for detection of residual or recurrent polyp. There are few studies that have examined the accuracy of advanced endoscopic imaging for the prediction of histological recurrence but none of these imaging modalities have been validated for surveillance after EMR. Therefore, current guidelines strongly recommend systematic biopsy of EMR scar. The main aim of this study is to assess the incremental benefit of narrow band imaging (NBI) and white light endoscopy (WLE) randomizing the initial technique for the endoscopic detection of post-EMR recurrence and to asses if this advanced imaging method achieve sufficient diagnostic accuracy to exclude recurrence without the need for biopsy.

NCT ID: NCT04239157 Recruiting - Clinical trials for Myelodysplastic Syndrome

A Phase II, Open-Label, Study of Subcutaneous Canakinumab, an Anti-IL-1β Human Monoclonal Antibody, for Patients With Low or Int-1 Risk IPSS/IPSS-R Myelodysplastic Syndromes and Chronic Myelomonocytic Leukemia

Start date: August 25, 2020
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well canakinumab works for the treatment of low- or intermediate-risk myelodysplastic syndrome or chronic myelomonocytic leukemia. Canakinumab is a monoclonal antibody that may interfere with the ability of cancer cells to grow and spread.

NCT ID: NCT04237740 Not yet recruiting - Clinical trials for Hepatocellular Carcinoma

Relenvatinib in the Tatment of Recurrence of Hepatocellular Carcinoma After Liver Transplantation

RRHCCLT
Start date: May 1, 2020
Phase: Phase 3
Study type: Interventional

The aim of this study is to evaluate the efficacy and safety of lenvatinib in the treatment of recurrence of hepatocellular carcinoma after liver transplantation.

NCT ID: NCT04237675 Recruiting - Surgery Clinical Trials

Postoperative Relapses in MS Patients

Start date: December 20, 2019
Phase:
Study type: Observational [Patient Registry]

The aim of the study is to record any relapses during one year postoperatively in patients and parturients diagnosed with MS who received general or regional anesthesia

NCT ID: NCT04233970 Completed - Clinical trials for Multiple Sclerosis, Relapsing-Remitting

Development and Evaluation of a Web-based Programme on Relapse Management for People With Multiple Sclerosis

POWER@MS2
Start date: February 17, 2020
Phase: N/A
Study type: Interventional

This randomized controlled trial will evaluate a web-based relapse management programme, which is easily accessible for people with multiple sclerosis. The trial is accompanied by a mixed-methods process evaluation and a health economic evaluation. It is expected that the programme will positively change patients' relapse management and strengthen their autonomy and participation.

NCT ID: NCT04231942 Recruiting - Varicose Veins Clinical Trials

Elastic Compression Stockings and Varicose Veins Recurrence

ECOS-VVR
Start date: December 16, 2019
Phase: N/A
Study type: Interventional

Hypothesis. Regular using of Class 1 below-knee graduated compression stockings (RAL GZ 387 standard) compared to the absence of elastic compression will reduce the risk of clinically significant varicose veins recurrence at 12 months after endovenous thermal ablation of the great saphenous vein and elimination of varicose tributaries.

NCT ID: NCT04230304 Active, not recruiting - Clinical trials for Recurrent Small Lymphocytic Lymphoma

Daratumumab and Ibrutinib for the Treatment of Relapsed or Refractory Chronic Lymphocytic Leukemia, DIRECT Study

Start date: September 16, 2020
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well daratumumab and ibrutinib work in treating patients with chronic lymphocytic leukemia that has come back (relapsed) or has not responded to previous treatment (refractory). Daratumumab is a monoclonal antibody which works with the body's immune system to destroy cancer cells. Ibrutinib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving daratumumab and ibrutinib may work better in treating patients with chronic lymphocytic leukemia compared to ibrutinib alone.

NCT ID: NCT04228315 Recruiting - Malaria Clinical Trials

Biomarkers of P. Vivax Relapse

Start date: November 19, 2019
Phase: N/A
Study type: Interventional

Plasmodium vivax malaria is difficult to manage because even after taking medicine that kills the infection in the blood, it can continue to hide quietly in the liver, later re-emerging into the blood and causing another episode of malaria illness (relapse). This clinical trial aims to enroll patient with P. vivax infections and try to detect signals in blood, urine and/or saliva coming from the silent liver stages to help identify who could benefit from treatment with primaquine. It also will explore if certain factors of patients negatively impact primaquine efficacy.

NCT ID: NCT04228263 Completed - Clinical trials for Unexplained Recurrent Miscarriage

Hydroxychloroquine and Unexplained Recurrent Miscarriage

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

Recurrent miscarriage affects women of childbearing age worldwide. Vascular endothelial dysfunction and immunological impairment are associated with recurrent miscarriage To date, there is no effective or optimal therapeutic approach for these condition. Hydroxychloroquine has endothelial protective action via ant diabetic, lipid lowering, antioxidant effects or direct endothelial protection. Hydroxychloroquine is an antimalarial and immunomodulatory agent. In pregnancy, hydroxychloroquine is prescribed for inflammatory conditions associated with adverse perinatal outcomes such as systemic lupus erythematosus, antiphospholipid syndrome and placental inflammatory lesions such as chronic histiocytic intervillositis, hydroxychloroquine has therapeutic potential to improve placental function in pregnancies associated with heightened inflammation.