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NCT ID: NCT05473572 Recruiting - Clinical trials for Developmental Stuttering

Effect of Stuttering Remediation Exercises on Cortical Auditory Evoked Potentials

Start date: August 17, 2021
Phase: N/A
Study type: Interventional

studying how the cortical auditory evoked potentials differ in children who stutter from who do not stutter and how these potentials change with therapy

NCT ID: NCT05473390 Recruiting - Stroke Clinical Trials

Effect of FES of Back Muscles on Spinal Posture and Gait in Hemiplegia

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

Hemiplegic patient have unbalanced posture because paralysis leads to muscle atrophy, which then causes an unbalanced alignment in the structure of spinal joints. Evaluation and therapy of postural alignment are important as early predictable factors in the overall daily function of stroke patients

NCT ID: NCT05471102 Recruiting - Placenta Accreta Clinical Trials

Ligation of Anterior Internal Iliac Artery With Conservative Management of Partial or Focal Placenta Accreta Spectrum

Start date: July 3, 2022
Phase: N/A
Study type: Interventional

The patients will be divided into 2 groups: Group (A) - Study group: Cases managed by lower segment resection with ligation of the anterior division of the internal iliac artery Group (B) - Control group: Cases managed by lower segment resection without ligation of the anterior division of the internal iliac artery The following operative details will be recorded: - Estimation of total blood loss - Pre and 24-h post-operative hemoglobin (g/dl). - The need for blood transfusion and its amount intra or postoperative will be recorded - Operative time and postoperative hospital stay will be recorded. - Close post-operative monitoring of the patients' vital signs, drain output, and urine output - Presence or absence of intraoperative complications; bladder, ureteric, bowel, or vascular injuries will be recorded. - Monitoring for postoperative morbidities

NCT ID: NCT05470998 Recruiting - Sickle Cell Disease Clinical Trials

L-Arginine in Children Having Sickle Cell Disease With Increased Tricuspid Regurgitant Jet Velocity

Start date: November 25, 2021
Phase: Phase 3
Study type: Interventional

This study aims to investigate the possible efficacy and safety of L-Arginine in children having Sickle Cell Disease with increased Tricuspid Regurgitant Jet Velocity

NCT ID: NCT05470166 Recruiting - Lidocaine Clinical Trials

Lidocaine Infusion With ERAS Protocol for Pancreatic Cancer Surgery: Effect on Pain and Patient Immunity.

ERAS
Start date: April 20, 2022
Phase: N/A
Study type: Interventional

The whole world now is directed to implement strategies that enhance the patient's quality of life and prevent tumor relapse. Enhanced recovery after pancreatic surgery (ERAPS) program was found to improve the quality of life as it is an evidence-based protocol designed to standardize and optimize perioperative medical care in order to reduce surgical trauma, perioperative physiological stress, organ dysfunction, reduction of clinical complications, length of hospital stay and the health costs together with increase of patient satisfaction. lidocaine; it is an amide local anaesthetic Recently its use as intravenous perioperative infusion for abdominal cancer surgeries is encouraging, as it significantly reduces postoperative pain, opioid consumption and nausea and vomiting. it also promotes gastrointestinal function recovery, and shortens the postoperative hospital stay. In addition, lidocaine in particular can act directly and indirectly on pancreatic cancer cells and the tumor microenvironment. The investigators suggest that IV lidocaine infusion in combination with ERAPS protocol may achieve better postoperative outcomes after pancreatic surgery for cancer.

NCT ID: NCT05466500 Recruiting - Clinical trials for Axillary Brachial Plexus Block

The Efficacy of Intravenous Dexamethasone on the Duration of Analgesia of Ultrasound Guided Axillary Brachial Plexus Block in Pediatric Patients Undergoing Below Elbow Orthopaedic Surgeries

Start date: July 26, 2022
Phase: N/A
Study type: Interventional

Postoperative pain is a common manifestation in orthopedic patients, mainly due to intraoperative tissue damage , inadequate intraoperative pain assessment and management. Axillary nerve block provides motor and sensory block with the distribution of the median, radial, ulnar and musculocutaneous branches so it can be conducted with upper limb orthopedic surgery in hand, rest and elbow surgery distal to the cubital fossa.Sensory blockade of the brachial plexus for perioperative analgesia leads to stable haemodynamics intraoperatively, smoother emergence from general anaesthesia and decreased need for supplemental analgesics or suppositories in the Post-operative period Intravenous (IV) dexamethasone has been used as an additive to local anesthetic for peripheral nerve blocks (PNBs) in adults with variable efficacy.To the best of our knowledge the efficacy of intravenous dexamethasone as adjuvant to bupivacaine in ultrasound guided axillary brachial plexus block in pediatrics has not been investigated In this study the investigators will assess the analgesic effect of adding intravenous dexamethasone to bupivacaine in ultrasound guided axillary block in children undergoing upper limb orthopedic surgeries. Objectives: - To determine the effect of adding intravenous dexamethasone on the duration of analgesia . - To determine the effect of adding intravenousdexamethasone on quality of analgesia

NCT ID: NCT05465967 Recruiting - Clinical trials for Quadratus Lumborum Block

Transmuscular Quadratus Lumborum Block on Post-Operative Analgesia After Total Hip Arthroplasty

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

The aim of this study is to compare between the post-operative analgesic effect of two approaches of transmuscular quadratus lumborum block (transverse versus paraspinous sagittal transmuscular QLB) in total hip replacement surgery.

NCT ID: NCT05465473 Recruiting - Clinical trials for Class II Division 1 Malocclusion

Effect of Low-level Laser Therapy During Maxillary Molar Distalization Using a Skeletally Anchored Appliance

Start date: December 12, 2021
Phase: N/A
Study type: Interventional

study will be directed to evaluate the effect of low-level laser therapy during maxillary molar distalization using a skeletally anchored appliance

NCT ID: NCT05465421 Recruiting - Decayed Teeth Clinical Trials

Effect of Bone Marrow Mononuclear Cell Layer Seeded on Platelet-rich Fibrin on an Alveolar Socket After Extraction

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

Bone marrow aspiration from maxillary tuberosity will be centrifuged to separate the bone marrow mononuclear cell layer using the density gradient separation method, then it will be seeded in a platelet-rich fibrin membrane and used for socket preservation to test the osteogenic ability of the bone marrow mononuclear cell layer in comparison to platelet-rich fibrin alone both ways will receive implant after 3 months

NCT ID: NCT05465369 Recruiting - Clinical trials for Discoloration, Tooth

Clinical Assessment of Injectable Flowable Composite With Giomer Technology vs High Viscosity Glass Ionomer Restorations in ART for Cancer Patients

Start date: January 20, 2023
Phase: N/A
Study type: Interventional

Aim of the Study: This study will compare between injectable flowable composite (Beautifil flow plus x) and high viscosity glass ionomer (Equia Fil) by ART caries preventive protocol in high caries risk patients receiving chemotherapy and/or radiotherapy