Clinical Trials Logo

Throat Pain clinical trials

View clinical trials related to Throat Pain.

Filter by:
  • None
  • Page 1

NCT ID: NCT06168981 Enrolling by invitation - Anxiety Clinical Trials

The Effect of Preoperative Chewing Gum on Anxiety and Sore Throat in Patients With Laryngeal Mask Airway

Start date: December 1, 2023
Phase: N/A
Study type: Interventional

This study was planned to investigate the effect of chewing gum in the preoperative period on patients' sore throat and anxiety levels.

NCT ID: NCT02894372 Completed - Mouth Diseases Clinical Trials

Faringomoss Effectiveness in Inhibiting Acute Throat Pain and Discomfort

Start date: January 2015
Phase: N/A
Study type: Interventional

The purpose of the study was to assess the effectiveness of Faringomoss in reducing the throat discomfort and pain in patients with acute throat diseases and postoperative patients after throat surgeries.

NCT ID: NCT01777854 Terminated - Clinical trials for Laryngopharyngeal Reflux

Anti-reflux Control to Decrease Post Tonsillectomy Pain

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

The study aims to determine if treating pediatric patients (age 7-17) for four weeks with omeprazole prior to tonsillectomy will decrease post tonsillectomy pain. The hypothesis is that many patients have silent laryngopharyngeal reflux and by reducing the acid entrance into the oropharynx, patients will have less post tonsillectomy pain due to decreased acid irritation of the surgical wound (tonsil fossas). The study will be a prospective double blind randomized study. Participants will be invited to participate in the study by giving the study information at the preoperative assessment, when the decision is made to have a tonsillectomy performed. If the patient agrees to participate in the study, a written consent and child assent will be obtained and the patient will be randomly assigned to a treatment versus control group based on the randomly assigned participant number. The treatment group will then be given a four week course of omeprazole to be taken for the four weeks prior to tonsillectomy. The patient will be given a post tonsillectomy assessment form. The form looks at postoperative pain (using a visual analog scale 1-10) as well as oral intake at postoperative day 0,1,3,5,7,10, and 14. The form will be turned in at the postoperative visit or mailed in. The pain level and oral intake between the two groups to will be compared to determine if antireflux control helps decrease the postoperative pain after tonsillectomy.

NCT ID: NCT01679366 Completed - Throat Pain Clinical Trials

The Effectiveness of Probiotics for the Therapy of Acute Pharyngotonsillitis in Adult Patients

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

The addition of probiotics to the routine therapy of Acute Pharyngotonsillitis in adult patients may shorten the duration, and reduce the severity of the disease.