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NCT ID: NCT06426745 Completed - Colonic Polyp Clinical Trials

Split-dose Versus Single-dose Bowel Preparation for Colonoscopy

Start date: November 1, 2022
Phase: N/A
Study type: Interventional

Colonoscopy is the current standard method for evaluation of colonic disorders such as colorectal cancer, IBD, polyps, and other conditions.

NCT ID: NCT06426719 Completed - Clinical trials for Alveolar Bone Resorption

Efficiency of Using Osseodensification Protocol

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

the goal of this clinical trial is to learn if the new osseo-densification technique works to provide enough bone width and quality prior to implant placement in the upper jaw the main question it aims to answer is: Is the use of osseo-densification protocol better than the standard alveolar ridge widening techniques; regarding efficiency and comfort in obtaining sufficient alveolar ridge width in horizontally atrophic alveolar ridges?

NCT ID: NCT06426199 Recruiting - TMJ Disc Disorder Clinical Trials

Chitosan-Hyaluronate Gel Mixture Vs Hyaluronic for Internal Derangement

TMJ
Start date: January 17, 2024
Phase: Phase 4
Study type: Interventional

This study is designed to assess the impact of injecting sodium hyaluronic acid versus a chitosan-hyaluronate hybrid gel into the upper compartment of the temporomandibular joint (TMJ) as a treatment for anterior disc displacement without reduction. The study will include patients diagnosed with Stage III or IV TMJ internal derangement (anterior disc displacement without reduction), as classified by Wilkes, with diagnoses confirmed through clinical symptoms and MRI evaluations. Participants will be randomly divided into two groups, both undergoing TMJ arthroscopy. In the first group, 2 ml of chitosan-hyaluronic acid hybrid gel will be injected into the affected joints, whereas in the second group, 2 ml of hyaluronic acid (HA) will be administered. The study will compare and analyze outcomes in both groups, focusing on pain during TMJ function, clicking sounds, the extent of maximum mouth opening, and maximum lateral jaw movement.

NCT ID: NCT06424496 Completed - Clinical trials for Postpartum Depression

Effect of Targeted Health Education Program on Nurses' Awareness About Postpartum Depression

PPD
Start date: February 28, 2024
Phase: N/A
Study type: Interventional

To assess nurses' knowledge of PPD at Ain Shams University Maternity Hospital and measure their knowledge level after an educational program on postpartum depression.

NCT ID: NCT06424457 Recruiting - Thoracic Empyema Clinical Trials

Pediatric Video Assisted Thoracoscopic Surgery (VATS) in Management of Empyema

VATS
Start date: April 1, 2024
Phase: N/A
Study type: Interventional

Thoracic surgeons have developed a thoracoscopic procedure which is less intrusive method allows complete evacuation and washing of the debris from the pleural cavity. This approach may also have the benefit of less invasive maneuver, a shorter hospital stay and a decreased rate of postoperative complications. The aim of this study is to evaluate the advantages and disadvantages of the video-assisted thoracoscopic surgery (VATS) approach in comparison with thoracotomy in management of empyema in pediatric patients.

NCT ID: NCT06424353 Recruiting - Postoperative Pain Clinical Trials

Postoperative Pain After Pulpectomy of Primary Molars

Start date: January 20, 2024
Phase: N/A
Study type: Interventional

Testing postopertive pain after pulpectomy of primary molars with endoflas using modified Wong-Baker scale of pain.

NCT ID: NCT06424093 Recruiting - Anxiety Clinical Trials

Effect of Virtual Reality Technology for Managment of Acute Pain in Outpatient Hysteroscopy

Start date: May 1, 2024
Phase: N/A
Study type: Interventional

Performing out patient diagnostic and operative gynecological procedures is becoming more popular having the benefits of reducing risks of general anaesthetia, decreasing healthcare burden and increasing satisfaction for both patient and provider. Virtual reality (VR), a new technology, has been studied as a distraction technique for non-pharmacological method of pain relief. It is a computer-generated representation of an immersive videos viewed through a headset.

NCT ID: NCT06424080 Recruiting - Clinical trials for Renal Cell Carcinoma

Oncological and Perioperative Outcomes of Laparoscopic Versus Robotic Partial Nephrectomy for Treatment of Renal Tumors.

Start date: May 1, 2024
Phase: N/A
Study type: Interventional

partial nephrectomy offers lower renal function impairment and equivalent oncological survival outcomes compared with radical nephrectomy in those with T1 tumors. As urology has embraced the gradual shift from open to minimally invasive surgery (MIS), PN is being completed more often by laparoscopic and robotic methods . The first laparoscopic transperitoneal partial nephrectomy was reported in 1993 by Winfield, with the retroperitoneal approach introduced 1 year later With advancing robotic technology and the development of the DaVinci system, urologists began to explore the realm of robotic-assisted urologic surgery. In 2004, Gettman et al. published a paper describing their experience with robotic-assisted laparoscopic partial nephrectomy. Moreover, robotic assisted partial nephrectomy (RAPN) and laparoscopic partial nephrectomy (LPN) seems to be significantly better than OPN in terms of perioperative complications, estimated blood loss and hospital stay. Conversely, transfusion rate, ischemia time, change in estimated glomerular filtration rate and early cancer outcomes are similar between the two approaches. International guidelines recommend the use of both approaches according to the surgeon and patient preferences. so, we are plaining to do the study comparing between RAPN and LPN regarding feasibility and ability of both techniques.

NCT ID: NCT06423859 Recruiting - Clinical trials for Post Operative Pain, Acute

Articaine Plus Dexmedetomidine in Supraclavicular Block

Start date: February 1, 2024
Phase: N/A
Study type: Interventional

Articaine has emerged as a local anesthetic (LA) that produces sensory and motor blockade shorter than bupivacaine and lower in neurotoxicity than lidocaine. Studies have shown that adding dexmedetomidine to LA produces prolongation of sensory and motor bock duration. Early regain of motor power with adequate analgesia is needed in ambulatory surgery, for early start of physiotherapy. This study was designed to test efficacy of adding dexmedetomidine to articaine on the duration of sensory and motor block.

NCT ID: NCT06423846 Completed - Clinical trials for Laparoscopic Sleeve Gastrectomy

Total Intravenous Anesthesia Versus Inhalation Anesthesia on Postoperative Liver Function

Start date: January 26, 2024
Phase: N/A
Study type: Interventional

The pandemic of obesity has become a serious issue of public health worldwide as the size of the obese population has almost tripled over the last four decades and continues to riseزThe epidemic of obesity has led to a significant increase in the prevalence of non-alcoholic fatty liver disease (NAFLD). NAFLD is currently the most common chronic liver disease, with an estimated global prevalence at 25-30%, rising up to 90% in morbidly obese patients