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NCT ID: NCT04393363 Active, not recruiting - Clinical trials for Chemotherapy-induced Peripheral Neuropathy

Early Detection of Neuropathy and Cognitive Impairment Following Treatment for Haematological Malignancies

NOVIT1
Start date: August 14, 2020
Phase:
Study type: Observational

Chemotherapy-induced peripheral neuropathy (CIPN) is a common, but not well understood complication to treatment with chemotherapy. In this study the investigators will investigate a novel method for early detection of CIPN and compare it to other methods in patients treated for haematological cancers.

NCT ID: NCT04201769 Active, not recruiting - Clinical trials for Chemotherapy-induced Nausea and Vomiting

Dexamethasone-sparing Approach Including NEPA Against Emesis Caused by Cisplatin

LUNG-NEPA
Start date: November 25, 2016
Phase: Phase 3
Study type: Interventional

This study evaluates the possibility to reduce the total dose of dexamethasone, when administered with NEPA, to prevent chemotherapy-induced nausea and vomiting (CINV) in Non-Small Cell Lung Cancer (NSCLC) patients receiving a cisplatin-based chemotherapy

NCT ID: NCT04201561 Active, not recruiting - Ovarian Cancer Clinical Trials

High Dose Inorganic Selenium for Preventing Chemotherapy Induced Peripheral Neuropathy

SELENIUM
Start date: December 24, 2019
Phase: Phase 3
Study type: Interventional

This study aims to evaluate the safety and efficacy of high dose inorganic selenium in preventing and relieving chemotherapy-induced peripheral neuropathy (CIPN) in platinum-sensitive recurrent ovarian, fallopian, or primary peritoneal cancer patients. This study will be conducted as a phase III randomized controlled trial in platinum-sensitive recurrent ovarian, fallopian, or primary peritoneal cancer patients who are expected to undergo paclitaxel-carboplatin chemotherapy. A total of 68 patients need to be enrolled in this study. The primary objective of this study is to evaluate the frequency of chemotherapy-induced peripheral neuropathy. The secondary objectives are the evaluation of the severity of peripheral neuropathy and the quality of life to show that selenium is effective in preventing and relieving peripheral neuropathy induced by paclitaxel. Positive results in this study will lead to further studies investigating the effect of selenium on other chemotherapies that can induce peripheral neuropathy.

NCT ID: NCT04167319 Active, not recruiting - Clinical trials for Chemotherapy-induced Peripheral Neuropathy

A Feasibility Study Investigating Chemotherapy-induced Neuropathy Using Multi-frequency Tactilometry and Patient-reported Outcomes (PRO)

CINCAN-1
Start date: November 20, 2019
Phase:
Study type: Observational

Chemotherapy induced peripheral neuropathy (CIPN) is among the most feared side effects to cancer treatment. The development of CIPN can lead to discontinuation or omission of antineoplastic drugs, possibly affecting efficacy of cancer treatment. There is a lack of knowledge about the natural course of CIPN and to this date, there are no available methods for the early detection of CIPN. With no effective prevention or treatment options, the condition has severe impact on patient quality of life and healthcare expenditure. This study will investigate the natural course of paclitaxel- and oxaliplatin induced peripheral neuropathy using novel diagnostic techniques. Multi-frequency vibrational technology has provided an objective method for the early detection of diabetic neuropathy. Our study will test the feasibility of this method within the field of clinical oncology and CIPN.

NCT ID: NCT04156698 Active, not recruiting - Immunotherapy Clinical Trials

Induction Chemotherapy Combined With Immunotherapy for Locally Advanced Hypopharyngeal Carcinoma

Start date: May 21, 2020
Phase: Phase 2
Study type: Interventional

This is a single-center, multidisciplinary, open-label, single-arm prospective clinical study.

NCT ID: NCT04112641 Active, not recruiting - Clinical trials for Chemotherapy-induced Peripheral Neuropathy

NIAGEN and Persistent Chemotherapy-Induced Peripheral Neuropathy

Start date: February 19, 2020
Phase: Phase 2
Study type: Interventional

The purpose of this randomized, double-blind, placebo-controlled, parallel group phase II trial is to determine whether nicotinamide riboside (NIAGEN®, NR) can ameliorate persistent peripheral neuropathy in cancer survivors who have completed chemotherapy with taxane or platinum-complex compounds between 1 and 12 months earlier.

NCT ID: NCT03984214 Active, not recruiting - Clinical trials for Chemotherapy-induced Nausea and Vomiting

Efficacy and Safety of Dronabinol in the Improvement of Chemotherapy-induced and Tumor-related Symptoms in Advanced Pancreatic Cancer

Start date: December 16, 2019
Phase: Phase 3
Study type: Interventional

Aim of this phase III trial is to investigate the efficacy and safety of dronabinol (orally administered tetrahydrocannabinol (THC)) as adjuvant therapy to first-line standard chemotherapy in patients with metastatic pancreatic cancer for improvement of chemotherapy- and tumor-related symptoms applicated by individual titration up to the maximum tolerated dose.

NCT ID: NCT03976882 Active, not recruiting - Clinical trials for Chemotherapy-Induced Thrombocytopenia

Hetrombopag for the Treatment of Chemotherapy-Induced Thrombocytopenia in Subjects With Malignancy.

Start date: November 6, 2019
Phase: Phase 3
Study type: Interventional

Randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of Hetrombopag in subjects with chemotherapy-induced thrombocytopenia receiving chemotherapy for the treatment of solid tumors.

NCT ID: NCT03620058 Active, not recruiting - Clinical trials for Refractory Acute Lymphoblastic Leukemia

CART22 Alone or in Combination With huCART19 for ALL

Start date: September 27, 2018
Phase: Phase 1
Study type: Interventional

This is a single center, open-label, phase 1 study to determine the safety and feasibility of infusing CART22-65s with or without huCART19 after administration of lymphodepleting chemotherapy in adult patients with relapsed or refractory B-ALL.

NCT ID: NCT03405324 Active, not recruiting - Clinical trials for Chemotherapy-induced Nausea and Vomiting

Effect of tDCS of the Motor Cortex on Chemotherapy Induced Nausia and Vomiting

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

this work is looking for the effect of tDCS of the motor cortex on the chemotherapy induced nausea and vomiting in cancer breast patients