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NCT ID: NCT04747678 Enrolling by invitation - Covid19 Clinical Trials

Adverse Effects of Ivermectin Used in Egypt During COVID-19

Start date: February 3, 2021
Phase:
Study type: Observational [Patient Registry]

retrograde study of common and rare adverse effects of multiple doses of ivermectin used during the coivd 19 pandemic in egypt

NCT ID: NCT04732364 Enrolling by invitation - Pain, Postoperative Clinical Trials

Analgesic Efficacy of Ultrasound Guided Erector Spinae Block for Modified Radical Mastectomy

Start date: April 30, 2018
Phase: Phase 2/Phase 3
Study type: Interventional

To compare the analgesic efficacy of dexmedetomidine and magnesium sulphate as adjuvants to levobupivacaine in erector spinae plane block in modified radical mastectomy surgery for acute and chronic pain management.

NCT ID: NCT04709315 Enrolling by invitation - Clinical trials for Rapid Sequence Induction

Rapid Sequence Induction: Succinyl Choline vs Rocuronium After Pretreatment With Dexmedetomidine

Start date: October 1, 2020
Phase: Phase 3
Study type: Interventional

Background: Rapid sequence induction is a well-established anesthetic procedure used in trauma setting and patients with full stomach. Succinyl choline has the been the drug of choice, however, it carries potential risk and sometimes fatal outcome. Aim of the study: to compare rocuronium after pre-treatment with Dexmedetomidine, to succinyl choline in providing excellent intubating conditions. Material and method: Patients were randomly allocated to one of two groups, of 120 each. Control (SS) group, patients received pretreatment with 10 ml 0.9% saline over 10 minutes, and succinyl choline 1mg/ kg was on induction. Experimental (DR) group, received pretreatment with Dex 1 µg / kg in 10 ml 0.9% saline over 10 minutes and rocuronium 0.6 mg/kg on induction.

NCT ID: NCT04686370 Enrolling by invitation - Complete Edentulism Clinical Trials

Effect of Different Implant Surface Treatments on Bony Changes Around Mandibular Implants

Start date: October 6, 2020
Phase: N/A
Study type: Interventional

The research will be conducted to report which type of surface treatment of dental implants that can be successful and aids in increasing bone to implant contact and how it affects the bony changes around the implants installed in mandibular arches for completely edentulous patients or whether there are specific precautions to be taken into consideration during implant planning concerned with the type of surface microstructure treatment and recommendations needed.

NCT ID: NCT04680663 Enrolling by invitation - Clinical trials for Peripheral Perfusion Index

Predictor of Postoperative Complications After Lengthy Surgical Procedures

Start date: January 1, 2021
Phase:
Study type: Observational [Patient Registry]

Many patients undergoing long time surgery will manifest increased level of blood lactate. Hyperlactacidemia can cause disturbance of internal environment, then leading to increased complications and longer ICU stay, even death. For postoperative patients, we must ensure adequate perfusion in order to minimize the length of hyperglycemia and improve patients' outcomes. With regard to lactate, it provides information about prefusion, but not timely enough for its delay on reflecting hypoperfusion. And it's not real-time and non-invasive. Peripheral perfusion index (PPI) is an indicator reflecting hypoperfusion in critical patients. It is measured using pulse co-oximetry technology which is characterized by being real-time and noninvasive. PPI is defined as "the ratio of pulsatile blood flow to the non-pulsatile blood flow", mirroring the strength of blood flow and quality of perfusion at sensor site, reflecting perfusion state of the body part . In contrast to lactate value, it's real-time and easy to monitor.

NCT ID: NCT04662021 Enrolling by invitation - Clinical trials for Anxiety Depression Disorder

Aerobic Training Versus Cognitive Behavioral Therapy in Management of Anxiety

Start date: December 10, 2020
Phase: N/A
Study type: Interventional

Anxiety and depression disorders (ADD) have the highest overall prevalence rate among psychiatric disorders in young females. Its manifestations are disabling, distressing a substantial negative impact on the quality of life. The purpose of this study was to compare the effect of cognitive-behavioral therapy and physical therapy on female students with mild to moderate anxiety and depression.

NCT ID: NCT04627389 Enrolling by invitation - Cleft Lip Clinical Trials

Orbicularis Oris Z-plasty Modification of Modified Millard Technique and the Esthetic Outcome of Cleft Lip Repair

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

This study aimed to evaluate the effect of orbicularis oris muscle z-plasty modification of modified Millard technique on the esthetic outcome and length of the repaired lip

NCT ID: NCT04590456 Enrolling by invitation - Hemophilia A Clinical Trials

Pulsed Electromagentic Field in Haemophilia

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

To assess the effect of pulsed electero- magnetic field on swelling, range of motion and muscle strength of hemarthrotic knee joints of haemophilic subjects.

NCT ID: NCT04575480 Enrolling by invitation - Ideal Time Interval Clinical Trials

The Ideal Time Interval Between Repeated Shock Wave Lithotripsy Sessions For Renal Stones: A Randomized Controlled Trial

Start date: July 15, 2020
Phase: N/A
Study type: Interventional

There is no consensus about the required time intervals between repeated SWL sessions applied for renal stones with some centers waiting for 3 days, others for one week and others up to one month to repeat lithotripsy. In the 2019 EUA guidelines stated that "There are no conclusive data on the intervals required between repeated SWL sessions. However, clinical experience indicates that repeat sessions are feasible (within 1 day for ureteral stones). The intense use of ESWL currently, the lack of knowledge about acute lesions caused by re-treatment within a short time interval and the empirical way by which treatment is conducted, stimulated us to search for a precise answers to the question What the ideal time interval between SWL sessions in the treatment of renal stone patients should be. This randomized controlled trial will be conducted at Urology and Nephrology Center in Mansoura, Egypt. Patients more than 18 years old with single primary renal stone fulfilling inclusion criteria will be randomly allocated to 3 groups (50 patients each).Group 1 will undergo SWL with 3 days between each session. Group 2 will undergo SWL with 7 days between each session and Group 3 will undergo SWL with 14 days between each session. Study parameters will be renal damage including the following items: - Tubular damage will be assessed through estimation of changes in urinary excretion of renal tubular enzyme kidney injury molecule 1(KIM-1). - Glomerular damage will be assessed by estimation of proteinuria and changes in GFR calculated by renal isotope scan. - Renal morphological and haemodynamic changes. - Treatment success is defined as clinically insignificant residual fragments less than 4 mm size.

NCT ID: NCT04566913 Enrolling by invitation - Clinical trials for To Assess Bucco-lingual Dimension of the Ridge While Using Pontic Shield Technique as a Treatment Modality for Ridge Preservation

The Use Of Pontic Shield Technique For Alveolar Ridge Preservation . A Case Series

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

To assess bucco-lingual dimension of the ridge while using pontic shield technique as a treatment modality for ridge preservation