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The Effect of Adding Pain Relievers to Local Anesthesia Before Preforming Drainage in Peritonsillar Abscess (pta)

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified October 2010 by HaEmek Medical Center, Israel.
Recruitment status was:  Not yet recruiting
Information provided by:
HaEmek Medical Center, Israel Identifier:
First received: October 21, 2010
Last updated: October 22, 2010
Last verified: October 2010
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 .

Condition Intervention
Peritonsillar Abscess
Drug: dypiron, tramadol

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Single Blind (Participant)
Primary Purpose: Treatment
Official Title: The Efficiency of DYPIRON and TRAMADOL in Addition to Local Anesthesia Prior to Incision and Drainage Procedure in Peritonsillar Abscess

Resource links provided by NLM:

Further study details as provided by HaEmek Medical Center, Israel:

Primary Outcome Measures:
  • the vas scale [ Time Frame: 40 min after giving the oral drugs ]

Estimated Enrollment: 32
Study Start Date: November 2011
Estimated Study Completion Date: December 2011
Estimated Primary Completion Date: November 2011 (Final data collection date for primary outcome measure)
Intervention Details:
    Drug: dypiron, tramadol
    dypiron 4 ML, tramadol 50 mg flashtab
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.


Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

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.

  Contacts and Locations
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Please refer to this study by its identifier: NCT01227200

Contact: shani fisher, RN BA 046494311 SUNSHAN2@GMAIL.COM

otolaryngology department, HaEmek mc Active, not recruiting
Afula, Israel
Otolaryngology department, HaEmek MC Not yet recruiting
Afula, Israel
Principal Investigator: Dror Ashkenazy, MD         
Sponsors and Collaborators
HaEmek Medical Center, Israel
  More Information

Responsible Party: orolaryngology department, HaEmek MC Identifier: NCT01227200     History of Changes
Other Study ID Numbers: emc100061ctil
Study First Received: October 21, 2010
Last Updated: October 22, 2010

Additional relevant MeSH terms:
Peritonsillar Abscess
Pathologic Processes
Pharyngeal Diseases
Stomatognathic Diseases
Respiratory Tract Infections
Respiratory Tract Diseases
Otorhinolaryngologic Diseases
Analgesics, Opioid
Central Nervous System Depressants
Physiological Effects of Drugs
Sensory System Agents
Peripheral Nervous System Agents processed this record on May 25, 2017