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Postoperative Complications clinical trials

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NCT ID: NCT04446520 Completed - Clinical trials for Postoperative Complications

Autogenic Drainage Effect on Blood Gases and Prevention of Pulmonary Complication After Upper Abdominal Surgery

Start date: June 27, 2020
Phase: N/A
Study type: Interventional

Purpose: This study will find out the effect of Autogenic drainage on the prevention of pulmonary complications after upper abdominal surgery. Method: Sixty patients post upper abdominal surgeries will be included, their ages ranged from 50 to 60 years old. The patients will be divided into two groups, study group (A) include patients that receive first traditional physiotherapy (localized breathing exercise, diaphragmatic breathing, and splinted coughing) then autogenic drainage (B)-Group B: patients that receive traditional physiotherapy (localized breathing exercise, diaphragmatic breathing and splinted coughing)

NCT ID: NCT04417790 Completed - Clinical trials for Congenital Heart Disease

Utility of Lung Ultrasound in the Estimation of Extravascular Lung Water in Pediatric Population

Start date: August 10, 2019
Phase:
Study type: Observational

Increased extravascular lung water (EVLW) may increase mortality and morbidity in cardiopulmonary pathology. Many factors can cause increased extravascular lung water and pulmonary edema after cardiac surgery. This includes left ventricular failure, acute mitral regurgitation; systemic inflammatory response post-cardiopulmonary bypass, left to right shunts, transfusion associated acute lung injury, acute respiratory distress syndrome(ARDS) and sepsis. The clinical assessment of lung water ranges from auscultation to radiological methods to invasive measurements like dye dilution or thermodilution studies. Lung ultrasonography is the newest modality for noninvasive assessment of extravascular lung water. Lung ultrasound has been validated against auscultation, chest X-rays, CT chest as well as the bedside gold standard, transpulmonary thermodilution in adults. Critically ill children are more susceptible to complications and worsened outcomes from increased EVLW. Lung ultrasound correlates with clinical and radiological endpoints, but has not been validated against invasive objective measures like transpulmonary thermodilution. Evaluation of transpulmonary thermodilution setups in the pediatric population has shown different normal values and cutoffs compared to adults, possibly due to differential rates growth and development. It is aimed to investigate the correlation of Lung ultrasound based indices of extravascular lung water to invasive measures, assess optimum cutoffs to appropriate clinical endpoints and evaluate their sensitivity and specificity.

NCT ID: NCT04402450 Completed - Postoperative Pain Clinical Trials

Suprainguinal Fascia Iliaca Block Versus PENG Block for Hip Arthroplasty Analgesia

Start date: August 31, 2020
Phase: N/A
Study type: Interventional

In recent years, suprainguinal fascia iliaca block (SFIB) has emerged as a reliable analgesic option for primary total hip arthroplasty (THA). In 2018, a new block was described, termed pericapsular nerve group block or PENG block, that selectively targets the articular branches of the femoral and obturator nerves while sparing their motor components. In this randomized trial, the investigators will compare US-guided SFIB and PENG block in patients undergoing primary THA. Since the main benefit of PENGB stems from its quadriceps-sparing effect, it was selected the incidence of quadriceps motor block (at 6 hours) as the primary outcome and the hypothesis that PENG block will result in significantly less motor block compared to SFIB.

NCT ID: NCT04373421 Completed - Clinical trials for Impacted Third Molar Tooth

Effect of St. John's Wort and Olive Oils on the Postoperative Complications

Start date: August 15, 2018
Phase: Phase 4
Study type: Interventional

Surgical removal of impacted third molars is one of the most frequent procedures carried out in the oral and maxillofacial surgery clinics. There are a varying range of postoperative complications including pain, edema and swelling. Antibiotics, analgesics and mouthwashes are usually prescribed for the treatment of these complications. Patients undergoing impacted third molar surgery are frequently prescribed chlorhexidine mouthwashes with/without benzydamine hydrochloride. However, to preclude the adverse effects of these chemical agents, there has been a search for plant-derived alternatives with anti-inflammatory, antibacterial and analgesic properties as part of the oral care routine following surgical removal of impacted third molars. However, there is no study investigating the comparison of different essential oils in the literature. Thus, this multicenter study was aimed to evaluate the effects of St. John's wort oil and virgin olive oil on the postoperative complications and compared with chlorhexidine gluconate plus benzydamine hydrochloride mouthwash after the removal of impacted wisdom teeth.This study was aimed to evaluate the effects of St. John's wort oil, virgin olive oil, and chlorhexidine gluconate plus benzydamine hydrochloride on the postoperative complications after the removal of impacted wisdom teeth.

NCT ID: NCT04371588 Completed - Clinical trials for Postoperative Complications

Perioperative Muscle Relaxant and Postoperative Outcomes

POMPO
Start date: March 17, 2018
Phase:
Study type: Observational

Muscle relaxant is usually needed for surgery. However, the optimal depth of neuro-muscular blockade is still on debate. Deep neuro-muscular blockade may benefit the patients during surgery, but may increase the risk of residual blockade after surgery. Residual blockade has been reported to increase risk of morbidity. In this study, we tend to observe the postoperative outcomes in patients undergoing abdominal surgery under general anesthesia. And to compare the outcomes in patients received different depth of neuro-muscular blockade.

NCT ID: NCT04364477 Completed - Pain, Postoperative Clinical Trials

TAP Block On Abdominal Surgery Patients With General Anesthesia

TAPBLOCK
Start date: January 4, 2015
Phase: N/A
Study type: Interventional

INTRODUCTION: The aim of this study was to investigate the effects of tranversus abdominis plane (TAP) block placed postoperatively using ultrasound guidance for patients with caesarean section, myomectomy and hysterectomy under general anesthesia by eliminating additional pain caused by surgical incision. MATERIALS AND METHODS: The study has been planned to investigate the postoperative analgesia of 50 patients with TAP blocks applied and non-applied between the ages of 18-65, who will pass abdominal surgery. Study has been conducted in a prospective, randomized and controlled manner. Patients have been classified as those who have undergone TAP block (group: I) and those without block (group: II).

NCT ID: NCT04357665 Completed - Clinical trials for Postoperative Complications

Laparoscopic Versus Open Repair of Bilateral Primary Inguinal Hernia

Start date: June 2014
Phase: N/A
Study type: Interventional

Currently, there is a controversy regarding the best approach for simultaneous repair of bilateral inguinal hernia. The aim of this study was to compare the outcome of laparoscopic versus open repair of bilateral inguinal hernia

NCT ID: NCT04343911 Completed - Clinical trials for Postoperative Complications

Postoperative Peripheral Neuropathy After Laparoscopic Colorectal Surgery

Start date: November 1, 2014
Phase: N/A
Study type: Interventional

This prospective cohort study of patients undergoing colorectal surgery positioned conventionally with shoulder braces was performed. After initial results the implementation of the Pink Pad ® took place in order to compare the two groups. This study favours Pink Pad over conventional positioning concerning postoperative neuropathy.

NCT ID: NCT04326088 Completed - Clinical trials for Head and Neck Cancer

Postoperative Complication After Free Flap Reconstruction for Head and Neck Cancer

Start date: April 1, 2018
Phase:
Study type: Observational

This study was designed to investigate the outcome of free-flap reconstruction surgery following head and neck cancer resection between primary and recurrent head and neck cancer patients.

NCT ID: NCT04307654 Completed - Clinical trials for Lactacidemia and Complications

Lactate and Complications in Cytoreduction Surgery for Peritoneal Carcinomatosis

Start date: January 2014
Phase:
Study type: Observational

Serum lactate is a risk factor for postoperative complications in patients undergoing cytoreduction surgery in peritoneal carcinomatosis