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

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ClinicalTrials.gov Identifier: NCT01227200
Recruitment Status : Unknown
Verified October 2010 by HaEmek Medical Center, Israel.
Recruitment status was:  Not yet recruiting
First Posted : October 25, 2010
Last Update Posted : October 25, 2010
Sponsor:
Information provided by:

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 .

Condition or disease Intervention/treatment
Peritonsillar Abscess Drug: dypiron, tramadol

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.


Study Design

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 32 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Single (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
Study Start Date : November 2011
Estimated Primary Completion Date : November 2011
Estimated Study Completion Date : December 2011

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Abscess Anesthesia
Drug Information available for: Tramadol
U.S. FDA Resources

Arms and Interventions

Intervention Details:
    Drug: dypiron, tramadol
    dypiron 4 ML, tramadol 50 mg flashtab

Outcome Measures

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

Eligibility Criteria

Information from the National Library of Medicine

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

Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01227200


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

Locations
Israel
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
ClinicalTrials.gov Identifier: NCT01227200     History of Changes
Other Study ID Numbers: emc100061ctil
First Posted: October 25, 2010    Key Record Dates
Last Update Posted: October 25, 2010
Last Verified: October 2010

Additional relevant MeSH terms:
Abscess
Peritonsillar Abscess
Suppuration
Infection
Inflammation
Pathologic Processes
Tonsillitis
Pharyngitis
Pharyngeal Diseases
Stomatognathic Diseases
Respiratory Tract Infections
Respiratory Tract Diseases
Otorhinolaryngologic Diseases
Tramadol
Analgesics, Opioid
Narcotics
Central Nervous System Depressants
Physiological Effects of Drugs
Analgesics
Sensory System Agents
Peripheral Nervous System Agents