Clinical Trials Logo

Pharyngitis clinical trials

View clinical trials related to Pharyngitis.

Filter by:

NCT ID: NCT03943186 Completed - Clinical trials for Acute Viral Pharyngitis

Application of Ectoin Containing Lozenges (EHT02) in Patients With Acute, Viral Pharyngitis.

Start date: December 13, 2018
Phase:
Study type: Observational

The goal of this non-interventional study is to investigate the safety, efficacy and tolerability of Ectoin Lozenges Honey Lemon (EHT02) compared to lozenges containing hyaluronic acid and islandic moss in the treatment of acute viral pharyngitis.

NCT ID: NCT03915561 Recruiting - Clinical trials for Postoperative Complications

Effect of Intravenous Dynastat on Postoperative Sore Throat

Start date: March 1, 2019
Phase: Phase 2
Study type: Interventional

A postoperative sore throat (POST) after tracheal intubation is one of the most common postoperative problems causing dissatisfaction to participants, including sore throat, dry throat, cough, sputum, hoarseness and even dysphagia. Both nonpharmacological and pharmacological measures have been attempted to alleviate the incidence and severity of POST with variable success. Airway inflammation may be important in the pathogenesis of these symptoms in intubated participants but however, there was still no study to investigate the effect of cyclooxygenase-2 (COX-2) for the prevention of POST. So, the investigators' study will be the first one to investigate if perioperatively intravenous (IV) Dynastat injection can be used as a new indication for POST prevention.

NCT ID: NCT03885752 Enrolling by invitation - Clinical trials for Postoperative Sore Throat

The Effects of Preoperatively Chewing Gum on Sore Throat After General Anaesthesia With a Laryngeal Mask

Start date: March 25, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Postoperative sore throat (POST) is an important problem after general anaesthesia. We assessed whether chewing gum preoperatively can reduce the incidence of POST after general anaesthesia administered via a streamlined liner of the pharyngeal airway (SLIPA).

NCT ID: NCT03846713 Recruiting - Clinical trials for Intubation Complication

Thermosoftening of Double-lumen Tube for Airway Exchanger Catheter

Start date: December 27, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effect of double-lumen tube thermal-softening before intubation on the success rate of tube exchange by airway exchange catheter.

NCT ID: NCT03805568 Completed - Clinical trials for Post Operative Sore Throat

A Postoperative Sore Throat After Thyroidectomy

Start date: July 5, 2017
Phase: N/A
Study type: Interventional

This study was performed to compare the effect on of a postoperative sore throat between dexmedetomidine and remifentanil in patients undergoing thyroidectomy.

NCT ID: NCT03792776 Not yet recruiting - Clinical trials for Postoperative Sore Throat

Effect of Lidocaine 1% and 2% in the Tube Cuff on Postoperative Sore Throat and Cough

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

Comparing the effect of different methods of endotracheal tube cuff inflation on the occurrence of a postoperative sore throat and cough (Air vs Lidocaine 1% vs Lidocaine 2%).

NCT ID: NCT03779516 Terminated - Sore Throat Clinical Trials

Effect of Nebulized Lidocaine on Postoperative Sore Throat

Start date: December 19, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to test the hypothesis that use of preoperative nebulized lidocaine is reduced the incidence of postoperative sore throat after endotracheal intubation.

NCT ID: NCT03777098 Completed - Clinical trials for Group A Streptococcal Infection

Pilot Study of Strepic® Device for the Diagnosis of Group A Streptococcal Pharyngitis

Start date: January 2, 2019
Phase:
Study type: Observational

The objective of this pilot study is to acquire images using the Strepic® device, a clinical prototype that has been designed specifically as a viable, low-cost, commercially realizable autofluorescence-based diagnostic test, using (1) fluorescence and (2) white light image data, as well as other clinical data points. By acquiring and analyzing the images of pharyngeal bacterial fluorescence and white light patterns in patients with Group A Streptococcus (GAS)-associated pharyngitis and comparing them with those observed in non-GAS pharyngitis, it is believed an algorithm can be developed such that the device will improve the ability of clinicians to quickly and accurately identify GAS infections.

NCT ID: NCT03768882 Completed - Sore Throat Clinical Trials

Comparison of the Efficacy of Intravenous Dexketoprofen and Paracetamol in the Treatment of Sore Throat

Start date: December 1, 2017
Phase: Phase 4
Study type: Interventional

Currently, paracetamol and nonsteroidal antiinflammatory drugs are widely used by emergency physicians in Turkey for the treatment of sore throat. The objective of the study is compare the efficacy of intravenous dexketoprofen and paracetamol in the treatment of the pain in patients presenting to the emergency department with sore throat

NCT ID: NCT03744832 Active, not recruiting - Pharyngitis Acute Clinical Trials

Point of Care Streptococcal Pharyngitis Testing

Start date: August 12, 2019
Phase: N/A
Study type: Interventional

Sore throat is a common problem in children typically caused by viral or bacterial infections. While viral infections resolve without treatment, bacterial infections, such as "strep throat," are treatable with antibiotics. Diagnosing "strep throat" traditionally required a throat swab for culture that delays treatment for several days. This may result in prolonged illness, activity absenteeism, and significant healthcare costs. New molecular tests can accurately diagnose "strep throat" within 8 minutes, but are more expensive and require impact evaluation before widespread implementation. This study will compare a new bedside molecular test with conventional throat cultures to evaluate for benefits to patients and families seen in the emergency department, as well to healthcare system operations. The investigators hypothesize that care for children and the associated healthcare costs will improve with these point of care molecular tests.