Reducing Post-tonsillectomy Pain by Tonsil Pillars Suturing.

Overview

comparing post-tonsillectomy pain with and without suturing tonsil pillars to investigate whether suturing tonsil pillars reduces the pain of post-tonsillectomy.

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Prevention
    • Masking: Single (Participant)
  • Study Primary Completion Date: June 1, 2020

Interventions

  • Procedure: tonsil pillars suturing
    • The technique of suturing the faucial pillars is used routinely as part of uvulopalatopharyngoplasty, after performing the tonsillectomy, with postsurgical haemorrhage occurring rarely.
  • Procedure: tonsillectomy without tonsil pillars suturing
    • tonsillectomy without The technique of suturing the faucial pillars is used routinely as part of uvulopalatopharyngoplasty, after performing the tonsillectomy, with postsurgical haemorrhage occurring rarely.

Arms, Groups and Cohorts

  • Active Comparator: patients with post – tonsillectomy suturing tonsil pillars
  • Placebo Comparator: patients without post – tonsillectomy suturing tonsil pillars

Clinical Trial Outcome Measures

Primary Measures

  • Reducing Post-tonsillectomy Pain by Tonsil Pillars Suturing.
    • Time Frame: 1 year
    • two patients’ group in this study , one group will have a Tonsil pillars suturing after the tonsillectomy and the second group will not have this technique after the tonsillectomy, then patience should answer a post pain tonsillectomy questionnaire , by the questionnaire and the checkups to compare how each group affected ( using SPSS program and Statistics Methods.

Participating in This Clinical Trial

Inclusion Criteria

1. Aged 18 and over. 2. patients with tonsillectomy indication due to chronic Tonsillitis. Exclusion Criteria:

1. patients with tonsillectomy indication without chronic tonsillitis ( due to other causes). 2. chronic disease, chronic neurology disease. 3. chronic psychology disease. 4. bleeding tendency.

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Hillel Yaffe Medical Center
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Contact(s)
    • Ronen Bar, MD, +972-52-9257123, ronen.n.bar@gmail.com

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