The Effect of Adding Pain Relievers to Local Anesthesia Before Preforming Drainage in Peritonsillar Abscess (pta)
Primary Purpose
Peritonsillar Abscess
Status
Unknown status
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
dypiron, tramadol
Sponsored by
About this trial
This is an interventional treatment trial for Peritonsillar Abscess
Eligibility Criteria
Inclusion Criteria:patients with PTA in ages 18-65, who agreed to join the research -
Exclusion Criteria:cave to dypiron and/or tramadol, pregnant women, mental illness,soldiers.
-
Sites / Locations
- otolaryngology department, HaEmek mc
- Otolaryngology department, HaEmek MC
Outcomes
Primary Outcome Measures
the vas scale
Secondary Outcome Measures
Full Information
NCT ID
NCT01227200
First Posted
October 21, 2010
Last Updated
October 22, 2010
Sponsor
HaEmek Medical Center, Israel
1. Study Identification
Unique Protocol Identification Number
NCT01227200
Brief Title
The Effect of Adding Pain Relievers to Local Anesthesia Before Preforming Drainage in Peritonsillar Abscess
Acronym
pta
Official Title
The Efficiency of DYPIRON and TRAMADOL in Addition to Local Anesthesia Prior to Incision and Drainage Procedure in Peritonsillar Abscess
Study Type
Interventional
2. Study Status
Record Verification Date
October 2010
Overall Recruitment Status
Unknown status
Study Start Date
November 2011 (undefined)
Primary Completion Date
November 2011 (Anticipated)
Study Completion Date
December 2011 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
HaEmek Medical Center, Israel
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to find if adding oral pain relievers as DYPIRON and TRAMADOL in addition to the local anesthesia injection, can help reducing the pain intensity in patients who diagnosed as Suffering from peritonsillar abscess (PTA)and treated by incision and drainage .
Detailed Description
Control group: the patient will get local anesthesia injection with Lidocain. After 5 minutes- the DR will preform the incision and drainage of the abscess.
Then the patient will be asked by the vas score, the the pain intensity that he feels.
Intervention group:the patient will get dypiron 4 ml and tramadol 50 mg. after 40 minutes,the patient will get local anesthesia injection with Lidocain. After 5 minutes- the DR will preform the incision and drainage of the abscess.then the patient will be asked by the vas score, the the pain intensity that he feels.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peritonsillar Abscess
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
32 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
dypiron, tramadol
Intervention Description
dypiron 4 ML, tramadol 50 mg flashtab
Primary Outcome Measure Information:
Title
the vas scale
Time Frame
40 min after giving the oral drugs
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:patients with PTA in ages 18-65, who agreed to join the research -
Exclusion Criteria:cave to dypiron and/or tramadol, pregnant women, mental illness,soldiers.
-
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
shani fisher, RN BA
Phone
046494311
Email
SUNSHAN2@GMAIL.COM
Facility Information:
Facility Name
otolaryngology department, HaEmek mc
City
Afula
Country
Israel
Facility Name
Otolaryngology department, HaEmek MC
City
Afula
Country
Israel
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dror Ashkenazy, MD
12. IPD Sharing Statement
Learn more about this trial
The Effect of Adding Pain Relievers to Local Anesthesia Before Preforming Drainage in Peritonsillar Abscess
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