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Complication clinical trials

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NCT ID: NCT02186964 Completed - Recurrence Clinical Trials

Comparison of Tension Free Primary Closure, Karydaks and Limberg Flap Methods

Start date: February 2011
Phase: N/A
Study type: Interventional

Pilonidal sinus is a chronic inflammatory disorder of intergluteal sulcus. The disease seen in between 15-35 years of age and 3-4 times more in males. The incidence of the disease is found as 8.8% in Turkish soldiers. The disorder mainly affects the quality of life. There are numerous methods in surgical treatment of Pilonidal sinus. The main difference in between those methods is the closing of the defect that occurs after the excision of the sinus tract. The defect can be closed by primary sutures or it can be left for secondary healing. Nowadays, the recurrence rate of flap procedures are lower therefore, flap procedures are commonly used. However, it has been reported that there is no difference between flap procedures and tension free primary closure. This result triggered the controversy that; if the healing side is tension free, midline suturing may have no importance. The aim of this study is to compare the results of 3 different surgical procedures used in treatment of pilonidal disease.

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: NCT01823328 Completed - Anesthesia Clinical Trials

Ketamine Versus Etomidate for Rapid Sequence Intubation

Start date: September 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the effectiveness and safety of ketamine and etomidate during rapid sequence intubation (RSI).

NCT ID: NCT01761474 Completed - Satisfaction Clinical Trials

CO2 Versus O2 Insufflation During ERCP Depending on Sedation Protocols

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

Endoscopic retrograde cholangiopancreatography(ERCP) and related procedures can cause abdominal pain and discomfort. Some clinical trials have indicated, using the visual analogue scale (VAS) score, that CO2 insufflation during ERCP ameliorates the suffering of patients without complications, compared with air insufflation. However, differences in patient suffering between CO2 and air insufflation after ERCP depending on sedation protocols have not been reported. We therefore planned prospective, double-blind, randomized, controlled study with CO2 and air insufflation during ERCP depending on sedation protocol.

NCT ID: NCT01743079 Completed - Chronic Hepatitis B Clinical Trials

Study of Telbivudine and Lamivudine to Prevent Vertical Transmission of Hepatitis B

Start date: January 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of telbivudine and lamivudine use during late pregnancy for the prevention of HBV perinatal transmission in highly viraemic mothers.

NCT ID: NCT01711957 Enrolling by invitation - Death Clinical Trials

The Perioperative Value of Platelet Counts in Predicting Outcome After Liver Transplantation

Start date: January 2008
Phase: N/A
Study type: Observational

Recent experimental and clinical studies have shown that platelets play a critical role in liver ischemia and regeneration. Thrombocytopenia, a frequent and potentially serious condition in liver transplantation (LT) recipients, was shown to be associated with postoperative morbidity and mortality after partial hepatectomy. The investigators aim at evaluating whether postoperative low platelet counts are indicators of short- and long-term outcomes after liver transplantation.

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: NCT01519362 Completed - Complication Clinical Trials

A Woman Suffered From Leukocytopenia and Widespread Migration After Polyacrylamide Hydrogel (PAAG) Injection in Epicranial Aponeurosis

Start date: October 2011
Phase: N/A
Study type: Observational

Polyacrylamide hydrogel (PAAG) has been used as an injectable filler for soft tissue augmentation in different parts of the body , such as face, breast , or even penis for more than a decade . However, there are never reports about the application of a large amount of PAAG in epicranial aponeurosis to change the contour of the upper cranium accompanied with leukocytopenia. This fancy application turned out to be a disaster for the women who suffered from leukocytopenia , widespread migration of PAAG, recurrent swelling of the affected tissues and temporal pain changing with the temperature and the facial expression .

NCT ID: NCT01466309 Enrolling by invitation - Complication Clinical Trials

Efficacy of Adjustable Thermoplastic Oral Appliances in Patient With OSA

ThaiSomnoguard
Start date: July 2011
Phase: N/A
Study type: Interventional

Somnoguard, a titratable-thermoplastic oral appliances for the treatment of OSA, has been reported its safety and efficacy in Caucasians at least in the short-term. However, there has been no reports in Thai patients. The objectives of this study is to investigate its efficacy and safety in Thai patients with OSA.