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

The recruitment status of this study is unknown because the information has not been verified recently.

Verified October 2010 by HaEmek Medical Center, Israel.
Recruitment status was Not yet recruiting

Sponsor:

Information provided by:

HaEmek Medical Center, Israel

ClinicalTrials.gov Identifier:

NCT01227200

First received: October 21, 2010

Last updated: October 22, 2010

Last verified: October 2010

History of Changes

Purpose

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 Endpoint Classification: Efficacy Study Intervention Model: Crossover Assignment Masking: Single Blind (Subject) 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:

Drug Information available for: Tramadol

U.S. FDA Resources

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 ] [ Designated as safety issue: Yes ]

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:

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.

Eligibility

Ages Eligible for Study:	18 Years to 65 Years
Genders Eligible for Study:	Both
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

Please refer to this study by its ClinicalTrials.gov identifier: 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

No publications provided

Responsible Party:	orolaryngology department, HaEmek MC
ClinicalTrials.gov Identifier:	NCT01227200 History of Changes
Other Study ID Numbers:	emc100061ctil
Study First Received:	October 21, 2010
Last Updated:	October 22, 2010
Health Authority:	Israel: Clalit Health Services

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

Anesthetics
Tramadol
Central Nervous System Depressants
Physiological Effects of Drugs
Pharmacologic Actions
Central Nervous System Agents
Therapeutic Uses
Narcotics
Analgesics
Sensory System Agents
Peripheral Nervous System Agents
Analgesics, Opioid

ClinicalTrials.gov processed this record on May 16, 2013

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