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Pharyngitis clinical trials

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NCT ID: NCT02160912 Completed - Acute Pharyngitis Clinical Trials

Non Interventional Study (NIS) Regarding the Application of Ectoin Mund- & Rachenspray in Patients With Acute Laryngitis and/or Acute Pharyngitis

Start date: February 2014
Phase: N/A
Study type: Observational

In this observational study insights regarding the tolerability and influence on the quality of life of the topical treatment Ectoin Mund- and Rachenspray compared to Emser Pastillen in patients with acute Pharyngitis/ Laryngitis under real life conditions shall be gained. Patients are treated with Ectoin Mund- & Rachenspray 1% or Emser Pastillen according to the demands of the physician and the instructions for use.

NCT ID: NCT02114021 Completed - Cough Clinical Trials

Effect of Betamethasone Gel and Lidocaine Jelly on Sore Throat, Cough and Hoarseness of

Start date: March 2012
Phase: Phase 3
Study type: Interventional

ABSTRACT: The aim of this study was to investigate the effect of betamethasone gel and lidocaine jelly (over tracheal tube cuff) compared with distilled water on the post intubation syndrome incidence. This study has not been carried out in Iran. 99 patients of either sex undergoing elective surgery were recruited in a single blind randomized study. The patients, using randomization table, were divided into three groups. Anesthetics and medications used during surgery were similar for all the patients. For the all patients, the incidence of postoperative sore throat, cough and hoarseness of the voice in the different follow-up periods (1, 6 and 24 hours) based on the different types of medications were obtained.

NCT ID: NCT02068469 Completed - Clinical trials for Streptococcal Sore Throat

In Vitro Diagnostic Device for the Detection of Strep A

Start date: December 2013
Phase: N/A
Study type: Observational

The purpose of this trial is to show the accuracy and specificity of the Liat analyzer and assay for detecting Strep A at the point of care lab compared to culture.

NCT ID: NCT02039427 Completed - Clinical trials for Anesthesia Intubation Complication

The Effect of Prophylactic Ketorolac on Sore Throat After Thyroid Surgery

Start date: January 2014
Phase: N/A
Study type: Interventional

Sore throat is one of most frequent complaints related to general anesthesia with tracheal intubation. Although sore throat is regarded as a minor and short-lasting discomfort after surgery, its incidence and intensity in high risk patients such as female gender, head and neck surgery and difficult laryngoscopy or intubation may attribute to prolong postoperative recovery and give patient dissatisfaction. Even though the pathophysiology of post-intubation airway symptoms is not completely clarified yet, the mucosal damage related inflammation at the cuff of endotracheal tube has been thought to be an essential trigger. Thus anti-inflammatory medication has been commonly used strategy to prevent postoperative airway discomfort after intubation. The preoperative administration of dexamethasone has been reported to reduce the incidence and severity of postoperative sore throat, but it is accompanied with the adverse effects such as hyperglycemia, delayed wound healing and increased infection in surgical patients. Ketorolac, non-steroidal anti-inflammatory drug (NSAID), is an analgesic that commonly used for postoperative pain control and has anti-inflammatory effect. Therefore, the investigator designed to evaluate the effect of ketorolac on sore throat in comparison to dexamethasone after thyroidectomy in female adult patients

NCT ID: NCT02033564 Completed - Postoperative Care Clinical Trials

Incidence of Sore Throat With Traditional Intubation Blades or Glidescope Blade

Start date: June 2012
Phase: N/A
Study type: Interventional

The purpose in this study is to determine whether there is a difference in the incidence of postoperative sore throat when using the GlideScopeā„¢ versus a traditional intubation blade involving patients that are not anticipated to have a difficult airway.

NCT ID: NCT01990781 Completed - Clinical trials for Postoperative Sore Throat, Cough, Hoarseness

Effect of Intravenous Lidocaine and Dexamethasone Combination on Postoperative Sore Throat, Cough and Hoarseness.

Start date: December 2013
Phase: Phase 4
Study type: Interventional

Post operative sore throat (POST) following tracheal intubation is a common problem causing dissatisfaction and discomfort to the patients. Prophylactic use of both lidocaine and dexamethasone has been used independently for this purpose. However, there is no study assessing the synergistic analgesic effects of lidocaine and dexamethasone for POST. The purpose of this study is to compare the effect of lidocaine, dexamethasone and lidocaine dexamethasone combination on the incidence and severity of POST.

NCT ID: NCT01986361 Completed - Sore Throat Clinical Trials

Placebo-Controlled Onset-of-Action Study of Flurbiprofen Utilizing the Double-Stopwatch Method

Start date: September 2013
Phase: Phase 3
Study type: Interventional

The study's purpose is to demonstrate the onset of action, i.e., time to meaningful pain relief in patients with pharyngitis, of flurbiprofen 8.75 mg lozenge using the Double-Stopwatch Method (DSW).

NCT ID: NCT01923831 Completed - Clinical trials for Post Operative Sore Throat

Comparison of the Effect of Magnesium Sulfate and Dexamethasone on Postoperative Sore Throat After Spinal Surgery in Prone Position With Tracheal Intubation: a Double-blind, Randomized, Noninferiority Clinical Trial

Start date: August 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effect of magnesium sulfate and dexamethasone on postoperative sore throat after spinal surgery in prone position with tracheal intubation.

NCT ID: NCT01806103 Completed - Pneumonia Clinical Trials

Antimicrobial Stewardship for Primary Care Pediatricians

PARTI
Start date: June 2010
Phase: N/A
Study type: Interventional

The purpose of the study is to determine if physician education coupled with audit and feedback of antibiotic prescribing can improve antibiotic prescribing by primary care clinicians.

NCT ID: NCT01785862 Completed - Clinical trials for Acute Sore Throat Pain

Ibuprofen Lozenge in Acute Sore Throat Pain

Start date: February 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of repeated doses of a low dosage of oromucosal Ibuprofen form (lozenge) versus placebo in patients suffering from acute sore throat pain.