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NCT ID: NCT05857293 Recruiting - Clinical trials for Neonatal Cyanosis Due to PDA Dependent Pulmonary Circulation

PDA Stent in Neonates With PDA Dependent Pulmonary Circulation

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

After echocardiography confirmation of PDA dependent pulmonary circulation in cyanotic neonates, catheter-guided PDA stent implantation will be done. Under general Anasthesia and after discontinuation of prostaglandin 4-6 hours before procedure, obtain vascular access and unfractionated heparin is given, then duct is accessed via a cut pig-tail or Judkins right [JR] catheter, and is crossed by PTCA wire to be carefully placed in the left or right branch pulmonary arteries, choose proper stent diameter and length, place the stent and confirm it's position, NICU admission for the neonate with heparin infusion for 24-48 hrs and acetylsalicylic acid is given then follow up the patient by pulse oximeter and echocardiography

NCT ID: NCT05857189 Recruiting - Orbital Deformity Clinical Trials

Quality-of-life Impact of Newly Formed Digitalized Printed Paper Inserted Into Eyeglasses

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

A straightforward, user-friendly removable orbital prosthesis is a practical choice for effective rehabilitation in such patients with defective eyes. One of the essential elements for a good recovery is the retention of the prosthesis. The prosthesis can be retained by using a spectacle frame, conformers, adhesives, osseointegrated implants, magnets, or buttons. Only osseointegrated prostheses in the maxillofacial region can use semi-precision attachments.

NCT ID: NCT05856279 Recruiting - Back Pain Clinical Trials

Immediate Effect of Two Selected Mulligan Techniques in Nonspecific Low Back Pain

Start date: January 16, 2023
Phase: N/A
Study type: Interventional

To compare between immediate effect of SNAG and mulligan lion position in range of motion (ROM) , pain, functional ability and kinesiophobia on patients with nonspecific low back pain.

NCT ID: NCT05856188 Recruiting - Clinical trials for Radiation-Induced Mucositis

Efficacy of Glutamine in Management of Radiation Mucositis

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

The goal of this [ type of study: Clinical trial] is to test effectiveness of glutamine in management of Radiation Induced Mucositis in head and neck cancer patients. The main question [s] ] is to [ learn about, test, compare etc.] it aims to answer are: 1. Is glutamine effective in management of Radiation Induced Mucositis? 2. Does Glutamine oral suspension affect the level of TGFβ1 in saliva of patients with radiation induced mucositis? participants will be asked to dissolve oral glutamine and maltodextrin in distalled water and swish and swallow three times daily during radiotherapy.

NCT ID: NCT05855460 Recruiting - Mycosis Fungoides Clinical Trials

Estimation of the Tissue and Serum Levels of Interleukin (IL) -35 in Mycosis Fungoides: a Case Control Study

Start date: January 12, 2023
Phase:
Study type: Observational

Tissue and serum samples from 20 MF patients and 20 normal healthy controls will be subjected for biochemical assessments by ELISA (Enzyme- linked immune-sorbent assay) for assessing the level of IL35.

NCT ID: NCT05855213 Recruiting - Respiratory Failure Clinical Trials

HVNI for Successful Weaning in Respiratory Failure

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

The goal of this randomized active-controlled study is to investigate the role of high velocity nasal insufflation (HVNI) in the immediate post-extubation period and compare it with non-invasive positive pressure ventilation (NIPPV) as regards to weaning success rate. The study will recruit those who have been on invasive mechanical ventilation for at least 3 days and with a high risk of weaning failure.

NCT ID: NCT05854511 Recruiting - HCV Clinical Trials

Pharmacokinetics, Safety, Efficacy and Acceptability of Daclatasvir Plus Sofosbuvir in HCV-infected Children

Start date: June 5, 2022
Phase: Phase 3
Study type: Interventional

This is an interventional, single center, single arm clinical trial to assess the pharmacokinetics, safety, efficacy, and acceptability of daclatasvir plus sofosbuvir in treatment-naïve children weighing between 14 and 35 kg with chronic HCV GT 1-6 infection.

NCT ID: NCT05852639 Recruiting - Clinical trials for Gestational Diabetes

Fetal CPR at Term for Prediction of Adverse Neonatal Outcome in Pregnancies Complicated by GDM

Start date: November 30, 2022
Phase:
Study type: Observational

The goal of this observational study is to evaluate fetal cerebroplacental ratio at term and its relation to adverse neonatal outcome in patients with gestational diabetes. The main question[s] it aims to answer are: - To evaluate the efficacy (sensitivity & specificity) of fetal cerebroplacental ratio at term in prediction of adverse neonatal outcome in pregnancies complicated by gestational diabetes - To evaluate the difference in fetal cerebroplacental ratio in patients treated by insulin & those on metformin - to evaluate the incidence of adverse neonatal outcome in patients treated by insulin & those on metformin. Participants will undergo ultrasound and doppler study at 37 weeks & every two weeks thereafter till delivery. Neonatal assessment will be done after delivery to exclude adverse outcomes.

NCT ID: NCT05851768 Recruiting - Analgesia Clinical Trials

Efficacy of Dexmedetomidine VS Magnesium Sulphate With Bupivacaine in Erector Spinae Block for Thoracotomy Pain

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

Postoperative pain management is considered an integral part of perioperative care in patients undergoing thoracotomy. In order to reduce these complications, multiple regional techniques have been developed for thoracotomy including Intercostal nerve block, Erectospinae plane block and serratus block. Multiple adjuvants have been used in regional analgesia including adrenaline,clonidine,magnesium sulphate,dexmedatomidine and opoids.

NCT ID: NCT05851612 Recruiting - Clinical trials for One Lung Ventilation

Comparison of Three Methods of PEEP Titration During One Lung Ventilation in Prone Position

Start date: June 5, 2023
Phase: N/A
Study type: Interventional

One-lung ventilation and prone positioning during thoracoscopic esophagectomy is associated with pulmonary complications so lung protection is strongly recommended. Individualization the optimal PEEP level according to the respira¬tory condition of patients has gradually attracted the attention of clinicians. The aim of this study is to compare and evaluate the differences between three different PEEP values in patients who will undergo thoracoscopic esophagectomy receiving either constant PEEP or driving pressure guided individualized PEEP or oxygenation guided individualized PEEP.