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NCT ID: NCT06369376 Completed - Clinical trials for New Nerve Conduction Protocol for Pectoral Nerve

Electrodiagnostic Approach for Pectoral Nerve Conduction Studies

Start date: June 30, 2023
Phase: N/A
Study type: Interventional

Anatomical studies have challenged traditional perceptions of the pectoral nerve structure, revealing a network of three branches rather than the previously accepted medial and lateral branches. This study aims to explore the implications of this updated anatomy on nerve conduction studies of the pectoral nerve and proposes a modified nerve conduction study protocol to enhance diagnostic accuracy. A study on 25 volunteers was conducted, examining the three parts of the pectoral nerve. Electrode placement followed a detailed methodology ensuring precise data collection. The nerve conduction study was performed bilaterally, exploring latency and amplitude while addressing inter-observer variability and demographic influences.

NCT ID: NCT06355869 Completed - Clinical trials for Spastic Cerebral Palsy

Repeatability of Gait Deviations in Children With Cerebral Palsy

Start date: August 17, 2021
Phase:
Study type: Observational

Three-dimensional gait analysis (3DGA) is the 'gold standard' for measurement and description of gait. Gait variability can arise from intrinsic and extrinsic factors and may vary between walking conditions. This study aimed to define the inter-trial (intrinsic) and inter-session (extrinsic) repeatability in gait analysis data of children with CP who were walking in four conditions, namely barefoot or with ankle-foot orthosis, and overground or treadmill.

NCT ID: NCT06355167 Completed - Clinical trials for Cardiovascular Diseases

Effect of Oral Intake of Bacopa Monneiri on Vascular Oxidative Stress

Bacoxy_I
Start date: March 15, 2022
Phase: N/A
Study type: Interventional

Bacoxy_I study aims to evaluate the efficacy of a standardized Bacopa monnieri extract, Bacopa-400®, on vascular oxidative stress.

NCT ID: NCT06340425 Completed - Cerebral Palsy Clinical Trials

The Effect of Selective Dorsal Rhizotomy on a Multidimensional Outcome Set in Children With Spastic Cerebral Palsy: a Retrospective Study

Start date: June 26, 2018
Phase:
Study type: Observational

Cerebral palsy or CP is the single largest cause of childhood physical disability, with a prevalence of 2-3 per 1000 livebirths. Children with CP experience different primary symptoms, including abnormal increased muscle tone or spasticity. Selective dorsal rhizotomy (SDR) is applied in children with spastic CP as a non-reversible tone reduction procedure. Better understanding of the effects of SDR on a multidimensional outcome set in one CP-cohort and on macroscopic muscle morphology can improve insights and clinical decision making.

NCT ID: NCT06321874 Completed - Abdominal Cancer Clinical Trials

Effects of Oxygen After Abdominal Oncological Surgery

EPHIRAS
Start date: January 1, 2011
Phase: N/A
Study type: Interventional

The aims of the research is to determine whether a Hyperoxic intermittent stimuli protocol can increase reticulocyte counts, signififying a rise in EPO production, in patients undergoing abdominal surgery

NCT ID: NCT06317090 Completed - Clinical trials for Alveolar Bone Resorption

Vertical GBR LPRF Block vs. Autogenous Bone With DBBM

Start date: July 2, 2018
Phase: N/A
Study type: Interventional

split-mouth RCT, 25 months follow up. GBR protocol with LPRF as grafting material in the test group and autogenous bone with DBBM as grafting material in the control group.

NCT ID: NCT06306235 Completed - Clinical trials for Cardiac Rehabilitation

Are Non-participants of Conventional Centre-based Cardiac Rehabilitation Willing to Participate in Cardiac Telerehabilitation?

Start date: October 12, 2020
Phase:
Study type: Observational

Patients who are eligible for cardiac rehabilitation but do not want to participate will be offered to participate in an interview (part A of the study) or a tablet questionnaire (part B of the study). Goal is to identify main barriers for conventional rehabilitation as well as to assess willingness to participate in cardiac telerehabilitation, main barriers and willingness-to-pay for cardiac telerehabilitation.

NCT ID: NCT06278792 Completed - Clinical trials for Acute Decompensated Heart Failure

Readily Available Urinary Sodium Analysis in Patients With Acute Decompensated Heart Failure

EASY-HF
Start date: March 7, 2022
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare physician-guided (SOC) versus nurse-led natriuresis-guided diuretic therapy in patients with acute decompensated heart failure (ADHF). The main questions it aims to answer are: - difference in natriuresis and diuresis - feasibility of the protocol. Participants will be asked to gather two 24 h urine collections. Researchers will compare SOC versus nurse-led diuretic titration to see if there is a difference in natriuresis after 48 hours.

NCT ID: NCT06268587 Completed - Postoperative Pain Clinical Trials

A Before and After Study Studying the Impact of an Analgesia Protocol After Discharge From Outpatient Surgery

Start date: September 1, 2019
Phase:
Study type: Observational

The goal of this before and after study is to measure the effectiveness of a home analgesia protocol after outpatient surgery in a tertiary hospital. The main question it aims to answer is: - Measure the impact of the protocol on the proportion of patients with a VAS greater than 3/10 on day one and who did not take the analgesics. The participants are divided into two groups. The control group leaves the hospital with instructions and prescriptions. The experimental group leaves the hospital with instructions, analgesics for a maximum of two days with detailed dosages and an explanatory booklet on postoperative pain.

NCT ID: NCT06267898 Completed - MDS Clinical Trials

Non Interventional Study on Iron Toxicity After First Allo-transplant in MDS/CMML

Start date: November 1, 2009
Phase:
Study type: Observational [Patient Registry]

Stem cell transplantation and blood product transfusions are standard of care for Myelodysplastic Syndromes (MDS). Several studies have shown changes in serum ferritin and non-transferrin-bound iron (NTBI) in patients undergoing stem cell transplantation. A large proportion of MDS patients are at risk for organ damage from tissue siderosis, due to the development of iron overload. Toxic effects of iron may play an important role in the complications associated with HSCT. Iron chelation therapy may reduce the acute and chronic treatment-related toxicity by removing excess of iron, iron radicals and reactive oxygen species (ROS). There is little information about the efficacy and safety of iron chelation in MDS patients. This audit wants to evaluate the effect of iron toxicity on treatment-related mortality in untreated, adult MDS or CMML patients during and after treatment with myeloablative conditioning (MAC) and reduced intensity conditioning (RIC) allo-HSCT, by prospectively collecting data from 200 MDS or CMML patients from 2009 onwards.