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NCT ID: NCT04852874 Recruiting - Local Anesthesia Clinical Trials

Quadratus Lumborum Block as an Anesthetic Method for Percutaneous Nephrolithotomy

Start date: April 3, 2021
Phase: N/A
Study type: Interventional

The study aims to investigate the efficacy and safety of QLB, as an anaesthetic method, for patients undergoing PCNL. Adult patients who agree to participate in the study will be included. Uncooperable patients, pregnant woman, active urinary tract infection, uncorrectable coagulation disorder, and those with known allergy to study medication will be excluded. Low dose spinal anaesthesia and Ultrasound-guided QLB will be performed. The success of the procedure, procedure-related complications, Intra- and post-operative hemodynamics, pain score, overall surgeon and patient satisfaction will be evaluated and reported.

NCT ID: NCT04852614 Recruiting - Clinical trials for Hepatitis C Virus Infection

Pharmacokinetics of Sofosbuvir/Daclatasvir in HCV-infected Lactating Women

Start date: December 1, 2020
Phase:
Study type: Observational

This is a prospective, observational, open-label, pharmacokinetic study will evaluate PK of SOF/DAC in lactating HCV-infected females at weaning or women who voluntarily decided to forego breastfeeding to initiate HCV infection treatment. Therefore, drug concentrations can be determined in maternal plasma and milk without risk to the children. HCV infected women at weaning after various durations of breastfeeding and HCV infected women who wish to initiate treatment immediately after delivery and forego breastfeeding will be recruited to start treatment under the guidance of their physician with SOF/DAC to determine M/P ratios of each of SOF, GS-331007 and DAC.

NCT ID: NCT04850365 Recruiting - Clinical trials for Pelvic Organ Prolapse

Abdominal Sacral Hysteropexy Versus Vaginal Sacrospinous Hysteropexy

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

The aim of the current study is to compare abdominal sacral cervicopexy with vaginal sacrospinous cervicopexy in women with apical prolapse in terms of operative time, procedures safety and efficacy.

NCT ID: NCT04849338 Recruiting - Clinical trials for Von Willebrand's Diseased Children, Bleeding Questionnaire is Done

The Role of Standardized Bleeding Score in Diagnosis of Pediatric Von Willebrand's Disease

Start date: April 15, 2021
Phase:
Study type: Observational

Von Willebrand's disease (VWD) is the most common inherited bleeding disorder. It arises from a deficiency in the quality or quantity of von Willebrand factor (VWF), a multimeric protein that is required for platelet adhesion. Typical patients present with mucocutaneous bleeding symptoms because of reduced circulating von Willebrand factor (VWF) In this study we will use the ISTH/SSC BLEEDING assessment tool as a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders

NCT ID: NCT04847700 Recruiting - Ménière Clinical Trials

Minimally Invasive Vestibular Neurectomy Versus Tenotomy of the Stapedius and Tensor Tympani Muscles in the Management of Patients With Unilateral Meniere's Disease

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

The distinctive symptoms of Meniere's disease (MD) include recurrent vertigo spells, fluctuating hearing loss, aural fullness and tinnitus. Conservative treatment in MD comprises lifestyle modifications, such as low-sodium diet, avoidance of caffeine, alcohol and stress, in addition to medication such as diuretics and betahistine. When conservative treatment fails, surgical management is attempted. Surgical interventions comprise transtympanic steroids or gentamicin, endolymphatic sac surgery (ES), ventilation tube placement, vestibular neurectomy, and labyrinthectomy. Recently, Loader et al. have presented encouraging results of the effectiveness of tenotomy of the stapedius and tensor tympani muscles (TSTM) in the management of patients with definite MD. Also, satisfactory results were obtained with endoscopic assisted minimally invasive vestibular neurectomy (MIVN). The aim of this study is to compare the clinical outcomes of MD patients who were submitted to either MIVN or TSTM in our department.

NCT ID: NCT04846621 Recruiting - Clinical trials for Preterm Labor With Preterm Delivery

Comparative Study Between Nicorandil and Nifedipine for the Treatment of Preterm Labour

Start date: June 1, 2020
Phase: Phase 2
Study type: Interventional

Nicorandil (potassium channel activator) is claimed to be as effective as Nifedipine (calcium channel blocker) for tocolysis in preterm labour aim of the study: To assess the efficacy of Nicorandil compared with Nifedipine as a tocolytic agent in delaying labour for 48 hours following their administration

NCT ID: NCT04846465 Recruiting - Urinary Stone Clinical Trials

Femoral Neck-shaft Angle in Sohag Population

NSA
Start date: September 14, 2021
Phase:
Study type: Observational

The femur or thigh bone is the strongest and longest bone of the body and about 45 cm long in an average man that means approximately one fourth of the height of individual. It has upper end, lower end and a cylindrical shaft. Upper end consists of head, neck. The neck is about 5 cm long, connects the head to the shaft and is directed upward, medially and slightly forward and making an angle about 125 with shaft but the angle is wider in children. The neck-shaft angle (NSA ) is defined as the angle formed by the neck axis and long axis of the shaft of femur.The knowledge of the neck shaft angle is valuable in the diagnosis and treatment of fracture of upper end of femur. The aim of the study is : 1. to evaluate the normal values of femoral neck-shaft angle 2. to detect factors that may affect this angle as age, and sex, in Egyptian adults from Sohag.

NCT ID: NCT04845061 Recruiting - Copd Clinical Trials

Evaluating the Outcome of Cardio Selective beta1- Blockers Use in Patients With Copd

Start date: October 1, 2021
Phase: Phase 4
Study type: Interventional

To Evaluate the Outcome of cardio selective beta1 (β1-) blockers use in patients with chronic obstructive pulmonary disease. Patient education about the COPD and their medications.

NCT ID: NCT04843826 Recruiting - Clinical trials for Papilla Reconstruction

Modified Pedicle Subepithelial Connective Tissue Graft for Interdental Papillary Reconstruction Around Delayed Implants in the Esthetic Zone: A Case Series Trail

delay implant
Start date: April 14, 2020
Phase: N/A
Study type: Interventional

This case series trial aims to evaluate the effect of a modified pedicle subepithelial connective tissue graft in creating anatomical papilla around one-stage delayed implant in the esthetic zone to establish better esthetics.

NCT ID: NCT04841564 Recruiting - Analgesia Clinical Trials

Open Versus Ultrasound Approach for Serratus Anterior Block

Start date: April 10, 2021
Phase: N/A
Study type: Interventional

Ultrasound-guided Serratus anterior plane (SAP) block is an interventional technique that recently gained popularity in the context of postoperative analgesia after breast surgery. Some limitations may be encountered during the use of ultrasound, such as obesity, tumor invasion of the surrounding muscles, which may lead to poor ultrasound image quality. The investigators hypothesized that an open approach to serratus anterior block by infiltration of local anesthetic between serratus anterior muscle and ribs after tumor excision during surgery would be non-inferior to ultrasound-guided approach where the primary endpoint of this prospective randomized blind controlled study will be the total dose of morphine consumed in the 1st postoperative 24 h. The patients will be randomly allocated to an open approach group and ultrasound approach group to serratus anterior block using computer-generated random numbers and sealed opaque envelops. For any statistical tests used results will be considered as statistically significant if P-value ≤0.05.