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Tonsillitis clinical trials

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NCT ID: NCT02571075 Completed - Tonsillitis Clinical Trials

Battlefield Auricular Acupuncture During Adult Tonsillectomies and Effect of Post op Pain and Nausea

BFA
Start date: November 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if auricular acupuncture significantly reduces post-operative pain in comparison to the standard of care. Post-operative pain score will be collected by subject self-report of pain according to the Numerical Rating Scale (NRS) (0= no pain, 10 = worst imaginable pain) up to 10 days post-operation.

NCT ID: NCT02183038 Completed - Pharyngitis Clinical Trials

Efficacy and Safety of Meloxicam vs. Naproxen Sodium in Patients With Acute Non Bacterial Pharyngitis or Pharyngo-tonsillitis

Start date: July 1998
Phase: Phase 2
Study type: Interventional

Study to assess the efficacy and tolerability of Meloxicam once daily dose of 7.5 mg and 15 mg compared with 1100 mg of naproxen sodium in the symptomatic treatment of acute non bacterial pharyngitis or pharyngo-tonsillitis, over a period of 5 days.

NCT ID: NCT01988558 Completed - Clinical trials for Recurrent Tonsillitis in Children

A Phase I/II to Assess Safety, Tolerability and Efficacy of DL-lactic Acid Syrup in Children With Recurrent Tonsillitis

Start date: December 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The study objectives are to evaluate Tonsitin™ (10% Lactic Acid) safety, tolerability and preliminary efficacy, as a potent treatment for Recurrent Tonsillitis in children.

NCT ID: NCT01790477 Completed - Clinical trials for Obstructive Sleep Apnea

Auricular Acupuncture for The Treatment of Post-Tonsillectomy Pain

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

The goal of this study is to assess the role of battlefield acupuncture in the reduction of pain scores status post adult tonsillectomy. Secondary goals of this study include reduction in narcotic usage, decreased nausea and vomiting, and evaluating patient factors that lend an increased risk of worsening pain or improved response with acupuncture.

NCT ID: NCT01721486 Completed - Airway Obstruction Clinical Trials

Acetaminophen's Efficacy For Post-operative Pain

Start date: September 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare IV acetaminophen to oral acetaminophen for pain control in children undergoing tonsillectomy with or without adenoidectomy.

NCT ID: NCT01695980 Completed - Clinical trials for Sleep Apnea, Obstructive

Laryngeal Mask Airway in Pediatric Adenotonsillectomy

LMA
Start date: August 2012
Phase: N/A
Study type: Interventional

The study will compare how often the tubing kinks when a LMA (laryngeal mask airway) with modified retractor is used compared to use of an endotracheal tube (ETT) and non modified retractor is used.

NCT ID: NCT01465009 Completed - Common Cold Clinical Trials

Placebo and Active Controlled Study to Compare the Efficacy of Aspirin and Paracetamol in Treatment of Sore Throat Associated With a Common Cold

Start date: November 2003
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the efficacy and safety of 1000 mg Aspirin (study medication) by comparing 1000 mg Paracetamol (study medication) in treating the symptoms of sore throat associated with a common cold. The study is designed to develop a treatment method against sore throat associated with a common cold which will have more advantages for patients than the methods that are currently available.

NCT ID: NCT01389349 Completed - Postoperative Pain Clinical Trials

Acupuncture for Tonsillectomy Pain

Start date: July 2011
Phase: N/A
Study type: Interventional

Pain after tonsillectomy can be severe and last ten days. Various new surgical instruments have been developed over the years in an attempt to reduce postoperative pain with mixed results and increased costs; no single tonsillectomy technique is superior to the rest. Patients are discharged to home usually on the day of surgery and often suffer significant pain and nausea. Pain medication is often prescribed which can cause nausea, vomiting and constipation. Children in pain are reluctant to take in fluids and may require intravenous hydration at an emergency department. "Battlefield acupuncture " has been recently developed by the US Air Force and is now being used in Iraq and Afghanistan on wounded warriors suffering severe acute pain from trauma. This protocol consists of five acupuncture points on the outer ear. A recent study has demonstrated decreased pain and agitation in children undergoing ear tube insertion. Ear tube patients have mild discomfort compared to tonsillectomy patients and are able to attend school the next day. The investigators have been encouraged by the benefits of acupuncture during surgery for ear tube patients and also wounded warriors recovering from their injuries. These findings motivated us to see if acupuncture during tonsillectomy surgery would result in less pain and nausea.

NCT ID: NCT01363531 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Clinical Trial for the Assessment of Delayed Antibiotic Treatment Strategies

PDA
Start date: December 2009
Phase: Phase 4
Study type: Interventional

The general hypothesis is that delayed antibiotic treatment strategies present similar effectiveness, when compared with non-prescription of antibiotics or the prescription of antibiotics, in the non-complicated acute respiratory tract infections.

NCT ID: NCT01361399 Completed - Common Cold Clinical Trials

Active and Placebo Controlled Study to Test the Efficacy and Safety of an Aspirin-Lidocaine Lozenge in the Symptomatic Treatment of Sore Throat Associated With a Common Cold

Start date: November 30, 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the analgesic efficacy of a single dose of a fixed combination of 500 mg Aspirin (Acetylsalicylic Acid) and 4 mg Lidocaine in adult patients with sore throat associated with a common cold in comparison to a single treatment with 500 mg Aspirin or 4 mg Lidocaine alone as well a Placebo (treatment without any active ingredient). The combination of Aspirin and Lidocaine in a single lozenge is expected to provide relief from sore throat pain by sequential action. A very fast inset of action will be achieved by the locally acting Lidocaine and a long duration of action will be achieved by the systemically acting Aspirin.