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Effects of Chemotherapy clinical trials

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NCT ID: NCT03840824 Completed - Clinical trials for Premature Ovarian Failure

Blood Spot Self-administered Test and Assay

Start date: October 2010
Phase:
Study type: Observational

The current study will compare hormone levels of AMH, FSH and inhibin B in blood specimens collected by venipuncture and fingerstick in a sample of pre-menopausal women ages 18-45 years with normal menstrual cycles.

NCT ID: NCT03402295 Completed - Multiple Myeloma Clinical Trials

Superiority of VCD Versus CTD in Patients With Newly Diagnose Multiple Myeloma Eligible for Transplantation

GBRAM003r
Start date: June 15, 2009
Phase: Phase 3
Study type: Interventional

This study compared two main different induction protocols used to treat myeloma eligible patients in Brazil. VCD against CTD.

NCT ID: NCT03197532 Completed - Clinical trials for Effects of Chemotherapy

Assessing Urinary Hormones in Female Cancer Survivors

AUHS
Start date: January 2011
Phase:
Study type: Observational

Women of late to mid reproductive age may participate in a study using novel methodology to identify subtle changes in the reproductive endocrine axis via daily urine hormone analysis, which may have important implications for reproduction and may signal reproductive senescence.

NCT ID: NCT02771470 Completed - Lung Cancer Clinical Trials

Intestinal Microflora in Lung Cancer After Chemotherapy

Start date: September 2014
Phase: Phase 1
Study type: Interventional

Probiotics modulate the gut microflora and immune status in lung cancer who need chemotherapy.

NCT ID: NCT02767388 Completed - Multiple Myeloma Clinical Trials

Electrophysiological Biomarkers of Chemotherapy-related Cognitive Impairment and Recovery

Chemobrain
Start date: September 1, 2016
Phase:
Study type: Observational

Broadly speaking, the goal of this study is to better understand the influence of chemotherapy treatment on the cognitive and neural mechanisms underlying human behavior. Extant literature lacks diversity in studied cancer populations and treatment protocols, and provides limited understanding of the cognitive abilities that are impaired by chemotherapy. To overcome these limitations, this study will employ a sophisticated battery of tests on an understudied cancer population. Eligible participants will either be patients diagnosed with hematological malignancy (HM) or demographically matched healthy control patients. After HM diagnosis and treatment protocols have been established, patients will be inducted into the longitudinal study comprised of three visits: 1) after diagnosis but prior to chemotherapy treatment (baseline), 2) after one treatment cycle (one month post-baseline), and 3) after three treatment cycles (three months post-baseline). Patients will undergo a test battery designed to measure specific behavioral and neural mechanisms of attention; tests will either be computer-based cognitive tasks or simulated driving tests that immerse patients into virtual driving scenarios. During each test, EEG will be concurrently measured through non-invasive scalp electrophysiology recordings; EEG recordings will reveal underlying neural mechanisms affected by chemotherapy. Additionally, neuropsychological tests of vision, attention, and memory will be administered, as well as questionnaires to evaluate health, mobility, and life space. Finally, blood samples will be collected to examine levels of circulating inflammation-specific proteins typically present in cancer patients. This study will allow us to better understand the mechanisms through which chemotherapy influences cognitive performance. Results from this study will influence the administration of chemotherapy treatments so that patients can continue to receive the highest medical care while maintaining optimal cognitive abilities and quality of life.

NCT ID: NCT02454673 Completed - Gastric Cancer Clinical Trials

Therapeutic Individualization for Patients With Locally Advanced Gastric and Gastroesophageal Cancer

Start date: September 2013
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate whether the R0 rate, pathological response degree, patterns of recurrence and long-term outcomes may be initially predicted in patients with locally advanced gastroesophageal junction and gastric cancer treated with a neoadjuvant approach and salvage surgery.

NCT ID: NCT02454647 Completed - Gastric Cancer Clinical Trials

Induction Chemotherapy, Chemoradiotherapy and Surgery in Locally Advanced Gastric Cancer Patients

Start date: September 2013
Phase: N/A
Study type: Observational

The aim of this study is to evaluate the efficacy of a neoadjuvant approach in patients with locally advanced gastric cancer and the identification of prognostic factors.

NCT ID: NCT02395341 Completed - Clinical trials for Effects of Chemotherapy

The Longitudinal Ovarian Reserve Study

Start date: May 2007
Phase: N/A
Study type: Observational

Postmenarchal female cancer patients scheduled to undergo cancer therapy may enroll in this study to assess changes in existing and novel surrogate measures of fertility potential before, during and after chemotherapy. Measures of fertility potential to be tested include ultrasound imaging for antral follicle counts and ovarian volumes, endocrine evaluation, and assessment of oxidative stress.

NCT ID: NCT02375776 Completed - Prostate Cancer Clinical Trials

Improving Outcomes in Cancer Patients on Oral Anti-Cancer Medications Using a Multi-modal Mobile Health Intervention

CORA
Start date: March 2015
Phase: N/A
Study type: Interventional

This study evaluates a smart phone based mobile application designed for patients with Renal Cell and Prostate Cancer taking oral anti-cancer medications. (OAMs) All participants will be patients at the Dana Farber Cancer Institute in Boston, Massachusetts. Half of the participants will use the mobile application for a 3 month period along with their usual care. Half of the participants will just receive usual care. The investigators hope to show that cancer patients taking OAMs who use the mobile application will be better connected to their care team and will develop increased competency for self-care which will primarily increase medication adherence.

NCT ID: NCT02324595 Completed - Clinical trials for Peritoneal Cavity Cancer

Minimally Invasive Interval Debulking Surgery in Ovarian Neoplasm: a Feasibility Study

MISSION
Start date: December 2013
Phase: Phase 2
Study type: Interventional

Phase II multicentric study