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NCT ID: NCT04685395 Active, not recruiting - Oral Mucositis Clinical Trials

Comparative Efficacy of Rebamipide Gargle And Benzydamine HCL Gargle in Prevention and Management of Chemo- and Radio-therapy-induced Oral Mucositis

Start date: December 26, 2019
Phase: Phase 3
Study type: Interventional

evaluate preventive and therapeutic effects of Rebamipide gargle on reducing incidence of oral mucositis in comparison with benzydamine HCL mouthwash.

NCT ID: NCT04684693 Active, not recruiting - Clinical trials for Rheumatoid Arthritis

Effect of Laser Puncture on Rheumatoid Arthritis Patients

Start date: December 25, 2020
Phase: N/A
Study type: Interventional

Studying the effect of laser puncture on rheumatoid arthritis patients

NCT ID: NCT04680078 Active, not recruiting - Epiphora Clinical Trials

Placement of Three Interrupted Sutures After Triangular Three-snip Punctoplasty

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

a prospective randomized study conducted upon 40 eyes of 24 patients with lower punctual stenosis (grade 1 or 2 according to Kashkouli scale) attending at Menoufia University hospitals and Kafr Elsheikh ophthalmic eye center. The upper punctum and canaliculus were patent. All patients were complaining of epiphora and had a thorough ophthalmological examination including dye disappearance test, and slit-lamp examination. A Nettelship dilator is used to enlarge the stenotic lacrimal punctum. A single blade of a small Westcott spring scissor or Vannus scissor is placed within the ampulla of the lacrimal canaliculus, with the remaining blade placed on the conjunctival surface of the posterior aspect of the eyelid. The first vertical snip is made at the vertical canaliculus. The second vertical snip is made from the edge of the first snip to create a flap. The final horizontal snip was made at the base. The triangular flap is removed and three sutures are placed, in an interrupted manner, at the posterior wall of the ampulla using 10-0 nylon. The sutures are removed 1 week after the surgery. Topical moxifloxacin 0.5% eye drops and fluorometholone 0.1% eye drops were used four times daily for one week.Patients were then followed up for 6 months after the surgery.

NCT ID: NCT04668456 Active, not recruiting - Clinical trials for Acute Postoperative Pain

Subtenon and Intravenous Dexmedetomidine Effect on Patients Undergoing Cataract Surgery

Start date: August 15, 2020
Phase: Phase 3
Study type: Interventional

The study designed to compare the effects and the safety of adding dexmedetomidine to local anesthetics and its intravenous administration in subtenon block in patients undergoing cataract surgery.

NCT ID: NCT04659720 Active, not recruiting - Clinical trials for Evaluations, Diagnostic Self

Clinical Evaluation of Stability of Dental Implant Placed Simultaneously With Closed Sinus Lifting Using Hydraulic Lift Technique Versus Summer's Osteotome Technique in Posterior Edentulous Maxilla (RCT)

Start date: October 27, 2020
Phase: N/A
Study type: Interventional

Clinical evaluation of stability of dental implant placed simultaneously with closed sinus lifting using hydraulic lift technique versus summer's osteotome technique in posterior edentulous maxilla (RCT)

NCT ID: NCT04648514 Active, not recruiting - Clinical trials for Evaluations, Diagnostic Self

Radiographic Evaluation of Bone Height Gain With Dental Implant Placed Simultaneously With Closed Sinus Lifting Using Hydraulic Lift Technique Versus Summers' Osteotome Technique in Posterior Edentulous Maxilla (RCT)

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

Radiographic evaluation of bone height gain with dental implant placed simultaneously with closed sinus lifting using hydraulic lift technique versus summers' osteotome technique in posterior edentulous maxilla (RCT)

NCT ID: NCT04643145 Active, not recruiting - Stones, Kidney Clinical Trials

Optimal Drainage After Flexible Ureterorenoscopy; Prospective Assessment of Perioperative Outcomes and Health-Related Quality of Life Through a Randomized Controlled Trial

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

Flexible ureterorenoscopy (FURS) is now recommended for the treatment of kidney stones smaller than 20 mm, as an alternative to extracorporeal shock wave lithotripsy (ESWL) and in combination with percutanous nephrolithotomy (PCNL) for stones larger than 20 mm. At the end of the operation, a ureteral drainage is put in place for the treatment of residual fragments and the inflammation following the ureteroscopy. It helps prevent obstructive symptoms and the development of strictures. Drainage is done either by a ureteral catheter or by a double J stent. In the literature, while drainage after ureteroscopy is recommended, the criteria for choosing between these two options are not clearly defined. The objective of this study will be to assess whether the type of postoperative drainage after URS for kidney stones can influence the perioperative outcomes and health-related quality of life.

NCT ID: NCT04641507 Active, not recruiting - Clinical trials for Lower Ureteric Stones

Comparative Study Between Tadalafil Versus Tamsulosin as a Medical Expulsive Therapy for Lower Ureteric Stones

Start date: January 1, 2020
Phase: Phase 4
Study type: Interventional

The aim of the work is to compare the efficacy of tadalafil and tamsulosin as a medical expulsive therapy for lower ureteric stones

NCT ID: NCT04635241 Active, not recruiting - Covid19 Clinical Trials

Inhaled Heparin for Hospitalised COVID-19 Patients

INHALE-HEP
Start date: June 1, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

This meta-trial is a prospective collaborative individual participant data meta-analysis of randomised controlled trials and early phase studies. Individual studies will be conducted in multiple countries, including Australia, the UK, the USA, Ireland, Argentina, Brazil and Egypt. Adult patients admitted to the hospital with confirmed SARS-CoV-2 infection, who do not require immediate mechanical ventilation, will be randomised to inhaled nebulised heparin or standard care for up to 21 days or until the patient has no respiratory symptoms. All studies will collect a minimum core dataset. The primary outcome for the meta-trial is the proportion of patients who receive invasive mechanical ventilation censored at day 28. Individual studies may have specific outcome measures in addition to the core set.

NCT ID: NCT04629001 Active, not recruiting - Clinical trials for Pregnancy Without Complications Except Getting Covid-19 Infection

Effect of Covid-19 on Outcomes of Pregnancy

Start date: September 1, 2020
Phase:
Study type: Observational [Patient Registry]

To study the effect of getting Covid-19 infection during pregnancy on the outcomes of the mother and the fetus including morbidity and mortality