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NCT ID: NCT06271486 Recruiting - Clinical trials for Postdural Puncture Headache

Pregabalin in Treatment of Postdural Puncture Headache

Start date: February 28, 2024
Phase: Phase 3
Study type: Interventional

Lumbar puncture (LP), often known as a "spinal tap," is a standard medical technique pioneered in the late 1900s by Heinrich Quincke. It involves the retrieval and analysis of cerebrospinal fluid (CSF) from the spinal cord, serving as the benchmark for diagnosing conditions like subarachnoid hemorrhage, meningitis, and specific neurological conditions. Pregabalin, an anticonvulsant medicine that blocks calcium entry, is used to treat a variety of diseases. It has been used to relieve pain in a variety of patient groups, including those with chronic pain, epilepsy, and anxiety disorders

NCT ID: NCT06271473 Recruiting - Safety Clinical Trials

Effect of PPV+ILM Peeling +/- Subretinal Injection of Ringer Lactate in Management of Nontractional Refractory DME

Start date: August 30, 2023
Phase: N/A
Study type: Interventional

To evaluate the efficacy and safety of combined pars plana vitrectomy and planned foveal detachment through subretinal injection of ringer's solution in patients with non-tractional refractory diabetic macular edema.

NCT ID: NCT06270550 Recruiting - Spastic Diplegia Clinical Trials

Role of Dynamic Movement Intervention in Children With Spastic Diplegia

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

The study aims to investigate the effect of dynamic movement intervention approach on static and dynamic balance, quality of step length and cadence of walking pattern of children with spastic diplegic cerebral palsy.

NCT ID: NCT06268548 Recruiting - Clinical trials for Diaphragm Dysfunction

Effect of Manual Diaphragmatic Activation on Diaphragm Function in Patients With Gastroesophageal Reflux Disease

Start date: September 15, 2023
Phase: N/A
Study type: Interventional

This study was conducted to investigate Effect of manual diaphragmatic activation on diaphragm function in patients with gastroesophageal reflux disease

NCT ID: NCT06268184 Recruiting - Oxidative Stress Clinical Trials

Effect of Omega 3 on Oxidative Stress and Nutritional Status of Children on Regular Dialysis

Start date: October 4, 2021
Phase: N/A
Study type: Interventional

evaluaion the effects of oral omega-3 supplementation on nutritional status and oxidative stress in pediatric patients with end stage renal disease on regular hemodialysis

NCT ID: NCT06267417 Recruiting - Oral Mucositis Clinical Trials

Laser Therapy Effect as Preventive Measure for Oral Mucositis in Children With Hematological Malignancies

Start date: April 10, 2023
Phase: N/A
Study type: Interventional

Introduction: Among the most drastic complications of chemotherapy is oral mucositis(OM). It is a painful inflammatory, often ulcerative condition and may increase risk for systemic infections leading to prolonged hospital stays and interruptions of treatment protocol. Many treatment modalities have been introduced for the prevention and treatment of oral mucositis , of which low level laser therapy(LLLT) is gaining popularity. The use of LLLT as a prophylactic treatment for chemotherapy induced oral mucositis in pediatric cancer patients is still lacking robust evidence. Also, the parameters used have not been optimized and no standard method has yet been established. Based on this point, this study will compare photobiomodulation to the conventional preventive program of oral mucositis applied in 57357 children's cancer hospital foundation to determine which will be optimal for the prophylaxis of chemotherapy-induced OM. Aim: To assess the effectiveness of low level laser therapy in the prophylaxis of oral mucositis in pediatric patients diagnosed with Hematological cancers. Methods: This study is a randomized, prospective, double-blinded trial that will include acute Myeloid leukemia patients admitted to receive chemotherapy cycle between the age of 3 and 18years. These patients will be randomized into two groups: group 1 will receive low level laser therapy and group 2 will receive mock treatment. Patient will be followed to asses the development of oral mucositis on prespecified time points.

NCT ID: NCT06266481 Recruiting - Clinical trials for Postoperative Sore Throat

Topical Dexamethasone Versus Topical Lidocaine Spray to Reduce POST in Shoulder Arthroscopic Surgeries: A Comparative Study

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

postoperative sore throat is the most frequent side effects after anaesthesia intubation. Dexamethasone and 10% lidocaine spray used prior to surgery has shown useful in managing these complications at the moment. In order to examine the prophylactic impact of local Dexamethasone and lidocaine on postoperative sore throat, this study was conducted.

NCT ID: NCT06265441 Recruiting - Postoperative Pain Clinical Trials

Comparison of Pain Relief Post Knee Arthroscopy Using IPACK + Adductor Canal Block vs. Adductor Canal Block Alone

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

In this study, the invistigators aim to compare postoperative analgesia effectiveness between combined interspace between the popliteal artery and posterior capsule of the knee block (IPACK) and Adductor canal block vs. Adductor canal block alone after Arthroscopic knee surgeries focusing on VAS score assessment at 8 hours postoperative.

NCT ID: NCT06265402 Recruiting - Block Clinical Trials

Retrolaminar Block Versus Tab Block in Abdomioasty

Start date: January 15, 2024
Phase: N/A
Study type: Interventional

The aim of the study is to compare the analgesic efficacy of Us guided retrolaminar block versus transversus abdominis plane block in patient under going abdominal plastic surgery

NCT ID: NCT06265116 Recruiting - Clinical trials for Dental Caries Class II

One-Step Universal Adhesives: A 3-year Clinical Trial in Class II Composite Restorations

Start date: January 23, 2024
Phase: N/A
Study type: Interventional

to evaluate and compare the clinical performance and periodontal responses of four commercially available one-step universal adhesives with different formulations in Class II composite restorations over a three-year period.