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NCT ID: NCT06423833 Recruiting - Clinical trials for High-Risk Surgical Patients

Trendelenburg Maneuver Versus Passive Leg Raising Test for Fluid Responsiveness in High-Risk Surgical Patients

Start date: February 1, 2023
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate whether Trendelenburg maneuver can be used to predict fluid responsiveness in high-risk surgical patients in intensive care unit as compared to Passive Leg Raising test.

NCT ID: NCT06423820 Recruiting - Clinical trials for Postoperative Nausea and Vomiting

Preoperative Ondansetron Lozenge for Prevention of Postoperative Nausea and Vomiting in Pediatrics Undergoing Squint Surgeries

Start date: May 21, 2024
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the role of ondansetron lozenge on prevention of postoperative nausea and vomiting (PONV) in pediatrics undergoing squint surgeries.

NCT ID: NCT06423807 Recruiting - Cesarean Section Clinical Trials

Preoperative Ondansetron Lozenge for Prevention of Post-Spinal Shivering in Caesarean Section

Start date: May 21, 2024
Phase: N/A
Study type: Interventional

The aim of this study is to estimate the role of ondansetron lozenge on prevention of post-spinal shivering in cesarean section.

NCT ID: NCT06423729 Recruiting - Clinical trials for Diabetes Mellitus, Type 2

Effect of Nicorandil in Type 2 Diabetic Obese Patients

Start date: June 1, 2024
Phase: Phase 2/Phase 3
Study type: Interventional

1. Evaluating the effect of nicorandil on glycemic control of diabetic obese patients treated with sulfonylureas. 2. Investigating the effect of nicorandil on body weight of diabetic obese patients treated with sulfonylureas.

NCT ID: NCT06423482 Recruiting - Clinical trials for Digitalization Accuracy

Digitization Accuracy and Scannability of Two Different Implant-Supported Prosthodontic Framework Materials

Start date: May 14, 2024
Phase: N/A
Study type: Interventional

The present study aims to clinically evaluate and compare the scanning accuracy and the scannability of 2 different materials used in constructing frameworks for implant-supported prosthesis (titanium and PEEK). The objective of the present study is to evaluate the digitization accuracy and scannability of milled titanium and PEEK implant-supported frameworks in intra-oral conditions and to evaluate the accuracy of the superstructures designed and constructed over the intraorally scanned framework.

NCT ID: NCT06423339 Recruiting - Post Operative Pain Clinical Trials

Comparison Between Genicular Nerve Block Combined With (IPACK) Block Versus Adductor Canal Block

Start date: May 10, 2024
Phase: N/A
Study type: Interventional

The patients will be randomized into 2 groups, named group A, B. Group A: The patients will receive Ultrasound guided Genicular nerves block combined with Ultrasound guided IPACK block. Group B: The patients will receive Adductor canal block which will be the control group. The Numerical Rating Scale (NRS) will be used to assess pain intensity. Preoperatively, all study subjects will be trained to use NRS pain scores. The spinal block will be performed. In group A, 15 mL of bupivacaine 0.25% with 2.5 g/mL adrenaline at a concentration 1:4,00,000 will be administered immediately following skin closure. GNB will be performed by using the linear ultrasound probe (10-15 MHz) Sono site M-turbo ultrasonography to scan the long bone shaft with up and down movement to recognize the epicondyle of the tibia and femur. The junctions between the epicondyle and the shafts of the femur and tibia are where the genicular arteries are located; these junctions will be defined as the periosteal areas. The superior lateral, superior medial and inferior medial genicular arteries accompany each genicular nerve. After confirmation of the genicular artery by color Doppler, the needle will be introduced using the in-plane approach and presented in the long axis view. The target point of the needle insertion will be the needle tip beside a genicular artery. Then, a 5 mL volume will be administered after gentle aspiration to prevent a faulty intra-arterial injection at 3 target locations: the superior lateral, superior medial and inferior medial genicular nerves. This will be Followed by the procedure for the IPACK block. In group B, A 22 Gauge 80 mm needle will be guided from lateral to medial to this area called the adductor canal using in-plane technique. 20 mL of 0.5% bupivacaine will be injected with peri-arterial spread after negative aspiration under sterile conditions. TKA will be performed by an orthopedic surgeon by placing three-compartment prostheses with a minimally invasive mini-midvastus approach and using hand-mixed cementing techniques.

NCT ID: NCT06422897 Recruiting - Corneal Perforation Clinical Trials

Role of AS-OCT in Assessment of Corneal Perforation

OCT
Start date: April 15, 2024
Phase:
Study type: Observational

Assessment of healing of thin and perforated cornea after surgical treatment by anterior segment optical coherence tomography

NCT ID: NCT06422559 Not yet recruiting - Depressive Disorder Clinical Trials

Accelerated Intermittent Theta Burst Stimulation in Unipolar Versus Bipolar Depression

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

The goal of this interventional study is to learn if accelerated Intermittent Theta Burst Stimulation can improve symptoms of 30 participants with Unipolar depression in higher manner than symptoms of 30 participants with bipolar depression

NCT ID: NCT06422286 Recruiting - Gagging Clinical Trials

Efficacy of Low-level Laser Acupuncture and Microcurrent Electrical Stimulation on Gag Reflex on Children

Start date: April 16, 2024
Phase: N/A
Study type: Interventional

the aim of the current study is to evaluate the effectiveness of the laser acupuncture in comparison to the electroacupuncure for controlling gag reflex in children

NCT ID: NCT06422260 Recruiting - Bone Loss Clinical Trials

Four-unit Implant Supported Fixed Partial Dentures Fabricated From Different Materials

Start date: January 19, 2023
Phase:
Study type: Observational [Patient Registry]

Implant supported superstructure is necessary for long term success and durability of the implant itself in terms of stresses distribution and fracture strength capability. Stresses falling on an implant are too much greater than those applied on a tooth structure with a periodontal ligament offering a degree of elasticity. The important mechanical and physical properties of materials used for the fabrication of dental prostheses include adequate flexural and tensile strength and modulus of elasticity, maximum fracture resistance, optimal bond strength and adequate polishability.