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NCT ID: NCT06460207 Not yet recruiting - Cognitive Training Clinical Trials

Neurofeedback Removal of Emotional Information From Mind

remtrain
Start date: September 2024
Phase: N/A
Study type: Interventional

This project will examine whether individuals can be trained, using real-time feedback about brain function during neuroimaging, to effectively remove thoughts from mind by providing them with a sense of what it feels like to successfully remove a thought.

NCT ID: NCT06459869 Not yet recruiting - Clinical trials for Locally Advanced Rectal Cancer (LARC)

NG-350A Plus Chemoradiotherapy for Locally Advanced Rectal Cancer

FORTRESS
Start date: November 15, 2024
Phase: Phase 1
Study type: Interventional

The FORTRESS trial (NG-350A-03) is an open-label, single-arm, and multicentre trial of NG-350A in combination with chemoradiotherapy (CRT) in adult patients with locally advanced rectal cancer (LARC) and at least one risk factor for local or distant recurrence.

NCT ID: NCT06459622 Not yet recruiting - Clinical trials for Chronic Rhinosinusitis With Nasal Polyps

Predictive Factors in Chronic Rhinosinusitis With Nasal Polyps

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

The study will be conducted to identify factors predicting the response of chronic rhinosinusitis with nasal polyps ( CRSwNP) to oral corticosteroids.

NCT ID: NCT06459193 Not yet recruiting - Clinical trials for Peripheral Neuropathy Due to Chemotherapy

Trimetazidine Efficacy in Attenuating Paclitaxel-Induced Peripheral Neuropathy

Start date: June 16, 2024
Phase: Phase 1/Phase 2
Study type: Interventional

This proof-of-concept study evaluated the effect of Trimetazidine on the incidence of paclitaxel-induced peripheral neuropathy in patients with breast cancer.

NCT ID: NCT06459115 Recruiting - Clinical trials for Acute Decompensated Heart Failure

Adherence to Medication in Patients With Acute Decompensated Heart Failure

ADHF-ED
Start date: February 1, 2023
Phase:
Study type: Observational [Patient Registry]

Every day, patients present to emergency department due to acute heart failure. There are many causes for decompensation. One possible cause is a lack of adherence to heart failure medication (prognosis-improving medications and diuretics). The aim of this study is to directly measure adherence in patients with acute heart failure (gold standard of adherence measurement using liquid chromatography coupled to high-resolution mass spectrometry= LC-HRMS/MS) at the emergency department. Questionnaires are used to investigate possible factors influencing adherence.

NCT ID: NCT06459024 Not yet recruiting - Clinical trials for Acute Myeloid Leukemia, in Relapse

Master Framework For Relapse or Refractory Acute Myeloid Leukemia

IMPACT STREAM
Start date: July 2024
Phase:
Study type: Observational

This is an observational (non-interventional), prospective, cohort study that will collects data from patients diagnosed with relapsed or refractory acute myeloid leukemia afferent to the participanting clinical sites

NCT ID: NCT06458855 Not yet recruiting - Prostate Cancer Clinical Trials

Nerve Grafting Technique to Restore Erectile Function Post Radical Prostatectomy

PRP-NR
Start date: June 2024
Phase: N/A
Study type: Interventional

A single arm prospective pilot trial evaluating the safety and the 1-year erectile recovery outcomes of patients undergoing a somatic to autonomic nerve grafting procedure for restoration of erectile function in patients who have lost erectile function following radical prostatectomy for prostate cancer. During this study a total of 10 patients who have persistent erectile dysfunction for more than 18 months post prostatectomy will undergo a post radical prostatectomy nerve restoration procedure (PRP-NR).

NCT ID: NCT06458842 Terminated - Narcotic Use Clinical Trials

Postoperative Pain Protocol Limiting Narcotics for Laparoscopic Hand-assisted Donor Nephrectomy

Start date: May 23, 2014
Phase: N/A
Study type: Interventional

Kidney donors represent healthy patients and their anticipated postoperative course should be uncomplicated and brief. This study looks to optimize the perioperative pain regimen of laparoscopic donor nephrectomy patients by minimizing or eliminating narcotics from the immediate post-operative period. Current postoperative standard of care after donor nephrectomy require narcotic analgesics. While narcotics are potent pain medications, they are often associated with complications including nausea, vomiting and dysfunction of the gastrointestinal tract causing prolonged complications. The investigators seek to evaluate a peri-operative pain regimen limiting the usage of narcotics. This incorporates a perioperative analgesic course utilizing combination of an intravenous non-steroidal anti-inflammatory drug (NSAID), intravenous acetaminophen, and intravenous ketamine. All three have been demonstrated to be effective for the control of perioperative pain while decreasing narcotics use. Prior to surgery, participants will be consented and randomly assigned to receive the standard of care perioperative pain management using intravenous narcotics as a patient-controlled analgesia (PCA) by itself plus placebo or along with the new protocol. The study will demonstrate it the new protocol will limit or eliminate the need for narcotics as a patient-controlled dose during the postoperative period. Upon discharge from the hospital, patients will be followed in clinic and via home questionnaires annually for 5 years to evaluate satisfaction, renal function and quality of life.

NCT ID: NCT06458439 Not yet recruiting - Clinical trials for Lymphoma, Non-Hodgkin

Epcoritamab-CAR T Cells for Large B-cell Lymphomas

Start date: July 2024
Phase: Phase 2
Study type: Interventional

This study investigates the feasibility and efficacy of epcoritamab treatment before CAR T cells. This study also investigates if, when patients have residual lymphoma after CAR T cells, epcoritamab can help to effectively treat that lymphoma.

NCT ID: NCT06458231 Recruiting - Clinical trials for Central Line-associated Bloodstream Infection (CLABSI)

Determining the Prevalence of Primary and Secondary Central Line Associated Blood Stream Infection (CLABSI) at the Tertiary Care Hospital

Microbiology
Start date: June 25, 2024
Phase:
Study type: Observational

- Review key history and clinical examination findings of cases with CLABSI. - Microbiological diagnosis and Culture sensitivity tests by automated Bact Alert and Vitek2c systems for CLABSI. - Determine antibiotic biogram of each organism isolated - Determine the prevalence of occurrence of Primary or secondary Blood stream infection, causing microorganism, and predisposing factors.