Reducing Post-tonsillectomy Pain by Tonsil Pillars Suturing.

Sponsor
Hillel Yaffe Medical Center (Other)
Overall Status
Unknown status
CT.gov ID
NCT04161196
Collaborator
(none)
40
2
12

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Procedure: tonsil pillars suturing
  • Procedure: tonsillectomy without tonsil pillars suturing
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Prevention
Official Title:
Reducing Post-tonsillectomy Pain by Tonsil Pillars Suturing.
Anticipated Study Start Date :
Dec 1, 2019
Anticipated Primary Completion Date :
Jun 1, 2020
Anticipated Study Completion Date :
Dec 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: patients with post - tonsillectomy suturing tonsil pillars

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.

Placebo Comparator: patients without post - tonsillectomy suturing tonsil pillars

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.

Outcome Measures

Primary Outcome Measures

  1. Reducing Post-tonsillectomy Pain by Tonsil Pillars Suturing. [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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Hillel Yaffe Medical Center

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hillel Yaffe Medical Center
ClinicalTrials.gov Identifier:
NCT04161196
Other Study ID Numbers:
  • 077-19-HYMC
First Posted:
Nov 13, 2019
Last Update Posted:
Nov 14, 2019
Last Verified:
Nov 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Nov 14, 2019