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NCT ID: NCT03771976 Completed - Clinical trials for Pregnancy Complications

Risk of Cesarean Section in Primiparous Women Over 35 Years of Age.

Start date: April 1, 2017
Phase:
Study type: Observational

The investigators reviewed Saint Thomas Maternity Hospital's database during a 5 year period and compared two cohorts of patients (primiparous women over 35 years of age and primiparous woman between 20 and 34 years of age). The objective was to determine the risk of cesarean section and other perinatal complications between the groups.

NCT ID: NCT03789305 Completed - Critical Illness Clinical Trials

Differences in Frail and Non-frail Critically-ill Patients in Functional Outcomes

DEFAULT
Start date: April 1, 2017
Phase:
Study type: Observational

This is a prospective analysis of patient registry data of intensive care patients. The aim is to investigate if frailty is a predictor of decline of functional status of critically ill patients during their hospital stay.

NCT ID: NCT03816670 Completed - Fertility Disorders Clinical Trials

Prospective Randomized Trial Comparing Corifollitropin-alfa Late Start vs. Corifollitropin-alfa Standard Start in Expected Poor, Normal and High-responders Undergoing IVF

Start date: April 1, 2017
Phase: N/A
Study type: Interventional

To compare the number of retrieved oocytes in the late start CF-alfa (day 4) versus standard CF-alfa protocols (day 2) in patients undergoing IVF. The primary analysis will be also performed in specific subgroups of patients: expected poor-responders, expected normal responders and expected hyper-responders

NCT ID: NCT03824002 Completed - Diabetes Mellitus Clinical Trials

Dulaglutide in Diabetic Patients, Relationship Between Arterial Stiffness, Endothelial Function, Clinical and Laboratory Variables

Start date: April 1, 2017
Phase: Phase 4
Study type: Interventional

The study aims to evaluate arterial stiffness and endothelial function indexes and their relationship with clinic and laboratory varible in a group of diabetic patients in treatment with dulaglutide

NCT ID: NCT03827304 Completed - Burns Clinical Trials

Using an Interactive Virtual Reality System to Distract Burns Patients During Burn Treatments

Start date: April 1, 2017
Phase: N/A
Study type: Interventional

The aims and objectives of the clinical feasibility trial are: - to investigate the potential for VR to reduced perceived pain and anxiety during painful dressings changes in a small sample of burns patients; - to measure the impact of the interventions on objective indicators of pain and distress during dressing changes within the small sample - to assess pain medication use during virtual reality interventions - to compare the above effects and experiences across two conditions within each participant: an active version of a virtual reality intervention, and a 'control' condition of no intervention; - to assess the perceived usability, acceptability, engagement with and enjoyment of the virtual reality intervention to the patients - to consider the apparent feasibility of the virtual reality intervention within a Burns Unit inpatient setting during painful dressing changes 4. Design This is an exploratory feasibility study with a small clinical sample of burns patients and staff caring for them, in a single burns unit setting, employing mixed methods and a repeated measures design to achieve the aims set out above.

NCT ID: NCT03828578 Completed - Clinical trials for Head and Neck Cancer

Comparison of AIRVO High Flow Oxygen Therapy With Standard Care for Prevention of PPCs After Major H&N Surgery

Start date: April 1, 2017
Phase: N/A
Study type: Interventional

Patients undergoing major head and neck surgery often develop breathing difficulties as a result of build up of sputum and difficulty taking deep breaths. Often as part of the surgery patients may also require a tracheotomy tube (a temporary tube placed into their airway) which is removed around 5-7 days after the operation. The presence of this tracheostomy tube increases the patient's risk of developing breathing problems, especially difficulty clearing sputum and reduced lung volumes. To reduce the risk of developing these problems, different forms of oxygen therapy and humidification are used. This normally involves using oxygen masks, nebulisers and other medications to help loosen the sputum and maintain blood oxygen levels. Another method of giving oxygen and humidification is through the use of AIRVO, which delivers the air / oxygen to the patient at higher rates as well as warming and humidifying the air. The aim of this study is to compare the AIRVO system to standard care in a small sample of patients (20 patients) undergoing major head and neck surgery involving insertion of a tracheostomy tube. The study will compare rates of breathing complications (e.g. pneumonia, reduced lung volume) as well as comparing the time to remove the tracheostomy tube and the time the patient is required to stay in hospital. These results will then be used to develop a larger funded study.

NCT ID: NCT03871218 Completed - Gingival Recession Clinical Trials

Effect of Hyaluronic-acid on the Healing After Free Gingival Graft

Start date: April 1, 2017
Phase: Phase 2
Study type: Interventional

This study evaluated the effect of topical hyaluronic acid (HA) application on free gingival graft (FGG) donor and recipient sites during the early wound healing period with laser Doppler flowmetry (LDF) and to investigate the effect of HA application on the dimensional change of the graft.Participants were randomly classified into the test group (TG) and control group (CG). HA was applied to both donor and recipient sites in 20 patients who formed the TG, whereas HA was not applied to the 20 patients who formed the CG.

NCT ID: NCT03875274 Completed - Postoperative Pain Clinical Trials

Morphine Added to Ropivacaine for FICB for Postoperative Analgesia

Start date: April 1, 2017
Phase: Phase 4
Study type: Interventional

prospective, randomized double blinded study to investigate the effects of morphine as an adjuvant to ropivacaine on FICB

NCT ID: NCT03881423 Completed - Muscle Relaxation Clinical Trials

Deep vs Moderate Neuromuscular Blockade in Day Case Laparoscopic Cholecystectomy.

Start date: April 1, 2017
Phase: Phase 4
Study type: Interventional

Laparoscopic cholecystectomy (LC) is commonly performed on ambulatory basis as a result of its ability to improve postoperative quality of recovery (QOR) and significantly reduce hospital stay .

NCT ID: NCT03892135 Completed - Clinical trials for Juvenile Idiopathic Arthritis

Representation and Medication Use in Juvenile Idiopathic Arthritis

RUMAJI
Start date: April 1, 2017
Phase:
Study type: Observational

According to the International League of Associations for Rheumatology classification, Juvenile Idiopathic Arthritis (JIA) comprises a heterogeneous group of arthritis of unknown cause and with onset before 16 years of age, characterized by joint inflammation lasting for 6 or more weeks. Few studies exist regarding the care experience of children affected by this rheumatic condition. On the other hand, methotrexate and biologics constitute the primary treatment for children with JIA. As with adults undergoing the same treatment, adherence is critical. Difficulties for children to take the drugs have been reported. Notwithstanding, if adherence promotion in pediatric chronic conditions has been the subject of recommendations with regard to care management, the investigators lack information to understand the grounds for adherence specifically in JIA. In order to understand and decipher the parent-child adherence mechanisms and practices, the RUMAJI study will be conducted. Indeed, improving the relational approach between children and their caregivers as well as unrestricted drug adherence involves researching and understanding how appropriation of the disease and treatment could be achieved.