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Complication clinical trials

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NCT ID: NCT03174509 Recruiting - Complication Clinical Trials

Is Positive Pressure Extubation a Safe Procedure?

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

Laboratory studies suggest extubation with positive pressure because it reduces the volume of secretions filtered into the distal airway. The aim of this non inferiority study is to evaluate the safety of the extubation technique under positive pressure with respect to the traditional technique (with suction and without positive pressure in the airways).

NCT ID: NCT03105713 Recruiting - Surgery Clinical Trials

Development and Implementation of Patient Safety Checklists Before, During and After In-hospital Surgery

PASC
Start date: November 1, 2021
Phase: N/A
Study type: Interventional

Building on the Norwegian Patient Safety Program's target areas, the Patients' Surgical Checklist (PASC) will empower surgical patients to become more involved in their own safety and contribute to preventive safety measures. A safety checklist for patients to use has been developed and validated for use in surgical patients. In a Stepped Wedge Cluster RCT effects of patients using their own checklists to avoid preventable patient harm are examined. The project will re-use existing health and personal data collected from patient records and patient reported data as outcome measures. A consortium of all relevant stakeholders and users participate: two hospitals with seven surgical clusters, patient representatives, representatives of general practitioners, and interdisciplinary in-hospital professionals. The important project partners are information and communications technology companies (Helse-Vest IKT and CheckWare service delivery), general practitioners, and national and international research partners leading in the field of patient safety, implementation science and health economics.

NCT ID: NCT03045965 Recruiting - Ovarian Cancer Clinical Trials

Hysterectomy and OPPortunistic SAlpingectomy

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

HOPPSA is a register based randomized controlled trial (R-RCT), with the objective to examine if opportunistic salpingectomy compared with no salpingectomy, at the time of hysterectomy for a benign reason - has no increased risk of complications - has no negative side effects on ovarian function and subsequent cardiovascular disease or incidence of fractures - implies reduced risk of subsequent ovarian cancer Randomization and follow-up will be conducted within national registers.

NCT ID: NCT02247778 Recruiting - Complication Clinical Trials

Surgical Innovations in Treatment of Clavicle Fractures

ClavFrac
Start date: April 2014
Phase: N/A
Study type: Interventional

Surgical incision for plate osteosynthesis of midshaft fractures of the clavicle averages 7 to 8 centimeters in the literature. It is hypothesized, that depending on the invasiveness of this incision secondary problems like prolonged fracture healing, paresthesia of supraclavicular nerves and pain due to scar tissue increase. Therefore we developed a mini-incision technique using an average incision length of 4cm. The aim of this study is to analyzed whether secondary problems following plate osteosynthesis of the clavicle correlate mit the length of the surgical access.

NCT ID: NCT02110628 Recruiting - Quality of Life Clinical Trials

Roux-en-Y vs. Roux-en-Y+ Pouch for D2 Total Gastrectomy

WCGCC-1202
Start date: August 2014
Phase: Phase 3
Study type: Interventional

Gastric is one of the most prevalence digestive malignance tumors in China. Radical resection of primary tumors and combine with dissection of regional lymph-nodes is acknowledged by surgeons all over the world. Nowadays, in order to improve the quality of life, controversies still exist to the reconstruction methods of total gastrectomy. Although roux-en-y anastomosis is the most common method adopted after total gastrectomy for it is an easily and safety method reconstruction method, but some problems still need us to solve, such as little food reserves, less food intake per meal and fast gastric emptying. These problems significantly affect the patients' quality of life after surgery. Roux-en-Y+Jejunal pouch anastomosis is newly born method can significant increase the volume to improve postoperative quality of life have been proven by some little sample size randomized control trail With the improvement of the gastric cancer surgery, this study proposed by prospective randomized controlled clinical trials aimed to comparing quality of life after traditional Roux-en-Y type and Roux-en-Y+ Jejunal pouch type anastomosis for radical total gastrectomy. Quality of life was evaluated according to the European Organization for Research and Treatment of Cancer (EORTC) Quality Of Life Questionnaire (QLQ)-C30 and QLQ-STO22. Quality of life will conducted in the 3 months, 6 months, 9 months, 12 months, 24 months, 36 months after gastrectomy.

NCT ID: NCT01849835 Recruiting - Complication Clinical Trials

A Test of the Comparison Between Trans-rectal and Trans-perineal Biopsy of Prostate

RCT
Start date: January 2013
Phase: N/A
Study type: Interventional

The purpose of this randomized controlled trial (RCT) is to compare the two ways (tras-rectal and trans-perineal) to perform prostate biopsy from the rate of Positive detection, complications, pain level, operation time and costs et al.

NCT ID: NCT01597869 Recruiting - Ultrasound Clinical Trials

Safety of Endobronchial Ultrasound-guided Transbronchial Needle Aspiration : A Prospective Study

Start date: April 2012
Phase: N/A
Study type: Observational

The purpose of this study is to find all kinds of complications and it's frequency related to the Endobronchial Ultrasound- Transbronchial Needle Aspiration (EBUS-TBNA) and to evaluate associated risk factors in patients who developed complications. The investigators performs EBUS-TBNA examination on all subjects that need mediastinal evaluation. All complications during or after the procedure will be recorded prospectively.

NCT ID: NCT01361477 Recruiting - Complication Clinical Trials

Data Registry of Intensive Care Unit (ICU) Siamitra and Intensive Care Unit (ICU) Salad-Samung

Start date: May 2011
Phase:
Study type: Observational

As a general surgical intensive care units of the biggest tertiary referral university of Thailand with more than 1,000 admissions/year, recently, more complicated perioperative care surgical patients were accepted with high complications, morbidities, mortality and resource utilization. Good data registration was needed to provide information for quality improvement and resource allocation. This prospective observational (crosssectional) study was designed to register patient > 18 years who will be admitted to these ICUs to explore the adequacy of these ICUs services, resource utilization (ICU length of stay and ventilator day), ICU complications, adverse outcome /ICU readmission within 72 hours after discharging from ICU. In addition, severe hemodynamic, respiratory, or neurological disturbance or complication intra and early postoperative (within 7 days after operation) that lead to ICU admission eg, intraoperative hypotension, intraoperative cardiac arrest, perioperative pulmonary aspirtaion will also be studied.