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NCT ID: NCT05463718 Recruiting - Clinical trials for Walking Performance in Spastic Hemiplegic Children

Virtual Reality Versus Balance Beam on Spastic Hemiplegic Cerebral Palsy

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

Is there any difference between the use of Virtual reality and Balance beam on walking performance in children with Spastic Hemiplegic Children?

NCT ID: NCT05462418 Recruiting - Incision, Surgical Clinical Trials

Diathermy vs Scalpel in Abdominal Incision in Women Undergoing CS

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

Cesarean section is surging worldwide. For an extended period of surgical practice, the scalpel has been well-known as a gold-standard tool for making surgical incisions. The diathermy, electrocautery, is a substitute.

NCT ID: NCT05460559 Recruiting - Stone, Kidney Clinical Trials

Endoscopic Combined Intrarenal Surgery Versus Multi-Tract Percutaneous Nephrolithotomy for Complex Renal Stones:

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

The aim of this study is to compare outcomes of endoscopic combined intrarenal surgery (ECIRS) with the multi-tract percutaneous nephrolithotomy for management of complex renal stones.

NCT ID: NCT05460442 Recruiting - Hip Surgery Clinical Trials

Pericapsular Nerve Group Block Versus Fascia Iliaca Block for Pediatric Hip Surgery

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

This compares the postoperative analgesic effect of ultrasound-guided pericapsular nerve group block (PENG) with ultrasound-guided fascia iliaca compartment block in pediatric patients undergoing hip surgery.

NCT ID: NCT05459792 Recruiting - Clinical trials for Radial Artery Cannulation

Comparative Study Between the Effect of Ultrasound Guided Median Nerve Block , Radial Nerve Block and Local Infiltration on Feasibility of Radial Artery Cannulation

Start date: July 18, 2022
Phase: N/A
Study type: Interventional

Arterial line placement is often needed in various critical care settings. It is a basic procedure performed for continuous blood pressure (BP) monitoring and rapid access for repeated arterial blood gas samples, as it is considered to be more precise than measurement of BP by other noninvasive devices, especially in the critically ill patients or those on continuous infusions of vasoactive drugs.Arterial line placement is presumed to be a relatively safe procedure, with a rate of major complications that is below 1%. The most common site of cannulation is the radial artery, primarily due to the ease of access owing to the superficial nature of the vessel and the ease with which the site can be maintained. Additional advantages of radial artery cannulation include anatomical reliability and the less complications. However placement of a radial artery catheter can, at times, be difficult because many patients who emergently need a catheter may have a weak arterial pulse due to dehydration or blood loss or may have some form of peripheral vascular disease. Although it is usually a well-tolerated procedure, it is considered more painful than intravenous (i.v.) cannula placement, particularly in case of multiple attempts of cannulation In this study the investigators will assess the effect of ultrasound guided median nerve block, radial nerve block and local infiltration with lidocaine on feasibility of radial artery cannulation in patients undergoing major surgeries Objectives 1. To evaluate the effect of ultrasound guided median nerve block, radial nerve block and local infiltration on feasibility of radial artery cannulation 2. To determine the effect of ultrasound guided median nerve block, radial nerve block and local infiltration in reducing discomfort and complicationassociated with radial arterial cannulation . 3. To evaluate the effect of ultrasound guided median nerve block, radial nerve block and local infiltration in radial artery diameter and blood flow for radial arterial cannulation

NCT ID: NCT05459701 Recruiting - Type 2 Diabetes Clinical Trials

Dapagliflozin in Type 2 Diabetes Mellitus Patients (T2DM) With Nonalcoholic Fatty Liver Disease (NAFLD)

Start date: May 1, 2022
Phase: Phase 4
Study type: Interventional

The aim of this study is to evaluate the effect of dapagliflozin on liver function of patient with NAFLD and T2DM.

NCT ID: NCT05457192 Recruiting - Clinical trials for Diabetic Polyneuropathy

Correlation of HbA1c With Electrophysiological Studies and Gait Performance in Diabetic Polyneuropathy Patients

Start date: July 2022
Phase:
Study type: Observational

This study will be conducted to investigate the relationship between glycosylated hemoglobin (HbA1c) and nerve conduction studies (NCS) with gait performance in patients with DPN. 65 patients with type II DM with moderate polyneuropathy will participate in this study. Glycosylated Hemoglobin (HbA1c) test will be done for each patient by using the Colorimeter device. Nerve conduction studies (NCS) will be performed for each patient by using the electromyography device to confirm the diagnosis of DPN. The neurophysiological functions of peripheral nerves including (The Common peroneal, Tibial, Sural, and Ulnar motor & sensory branches) will be measured. Spatiotemporal gait parameters (stride length, cadence& velocity) for all the patients will be assessed by two-dimension video-based motion analysis (2D).

NCT ID: NCT05455983 Recruiting - COVID-19 Vaccine Clinical Trials

COVID-19 Vaccine and Development of Immune Thrombocytopenic Purpura

Start date: August 1, 2022
Phase:
Study type: Observational

Detect development of immune thrombocytopenic purpura (ITP) after different types of (COVID-19) vaccination

NCT ID: NCT05455788 Recruiting - Clinical trials for Prosthetic Valve Endocarditis

Prosthetic Valve Sweing Ring Injection by Antiboitics Can Affect the Rate of Postoperative Infective Endocarditis?

Start date: December 1, 2021
Phase:
Study type: Observational

Follow-up of patients undergoing cardiac valve replacements with prosthetic valve after injection of sewing ring of prosthetic valve with aminoglycoside for prevention of infective endocarditis.

NCT ID: NCT05455723 Recruiting - Airway Management Clinical Trials

Tracheal Tube Cuff Inflation-Deflation Method for Video Assisted Laryngoscope Nasal Intubation in Adults

Start date: January 19, 2022
Phase: N/A
Study type: Interventional

Magill forceps is used to maneuver the endotracheal tube ETT in the posterior oropharynx and place its tip into the laryngeal inlet. While the Magill forceps are useful in guiding the nasotracheal tube past the vocal cords, care must be taken to avoid excessive maneuvering in order to minimize the risk of local trauma and rupture of the nasotracheal tube balloon. Cuff inflation-deflation method can reduce the apnea time in the adult patients. This, in turn, could point to a reduction in the complications (as desaturation and cardiac arrhythmia) that associated with the prolonged-time procedure.