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Wound Healing and Pain Management in Partial Thickness Burns

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 January 2011 by Rabin Medical Center.
Recruitment status was:  Not yet recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01289340
First Posted: February 3, 2011
Last Update Posted: February 3, 2011
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Rabin Medical Center
  Purpose
the aim of the study is to compare between two advanced wound dressing and conventional dressing for the primary ER treatment of superficial partial thickness burns

Condition
Pain

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Pain Management and Wound Healing in Partial Thickness Burn: Comparative, Post Marketing, Observational Trail Comparing Advanced Foam Dressings to Conventional Treatment.

Resource links provided by NLM:


Further study details as provided by Rabin Medical Center:

Primary Outcome Measures:
  • complete wound healing [ Time Frame: up to two to three weeks ]
    final burn wound closure


Estimated Enrollment: 100
Study Start Date: March 2011
Estimated Study Completion Date: March 2014
Estimated Primary Completion Date: March 2013 (Final data collection date for primary outcome measure)
Groups/Cohorts
Polymem (R)
superficial burns treated with Polymem wound dressing until complete wound healing
Biaten IBU
burns treated with Biaten IBU until complete wound healing.
Hartmen dressing
burns treated with hartman or saline wet dressing until wound healing

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years to 40 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
patients ages 18-40 with no co-morbidities nor pregnant.
Criteria

Inclusion Criteria:

patients with minor superficial partial thickness burns

Exclusion Criteria:

co-morbidities, pregnancy

  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): NCT01289340


Contacts
Contact: Dean D Ad El, MD 9376371 deana@clalait.org.il
Contact: Asaf Olshinka, MD 9376366 asafol@clalit.org.il

Locations
Israel
Beilinson hospital, RMC Not yet recruiting
Petah tikva, Israel, 49100
Sub-Investigator: Asaf Olshinka, MD         
Sponsors and Collaborators
Rabin Medical Center
Investigators
Principal Investigator: Dean D Ad El, MD Rabin medcial Center
  More Information

Responsible Party: Dean D. Ad-El M.D., Rabin Medical Center
ClinicalTrials.gov Identifier: NCT01289340     History of Changes
Other Study ID Numbers: 6021rmc
First Submitted: February 2, 2011
First Posted: February 3, 2011
Last Update Posted: February 3, 2011
Last Verified: January 2011

Keywords provided by Rabin Medical Center:
wound healing
pain
burn