Wound Healing and Pain Management in Partial Thickness Burns
This study is not yet open for participant recruitment.
Verified January 2011 by Rabin Medical Center
Sponsor:
Rabin Medical Center
Information provided by:
Rabin Medical Center
ClinicalTrials.gov Identifier:
NCT01289340
First received: February 2, 2011
Last updated: NA
Last verified: January 2011
History: No changes posted
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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 ] [ Designated as safety issue: No ]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| Ages Eligible for Study: | 18 Years to 40 Years |
| Genders Eligible for Study: | Both |
| 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
Please refer to this study by its ClinicalTrials.gov identifier: 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
No publications provided
| Responsible Party: | Dean D. Ad-El M.D., Rabin Medical Center |
| ClinicalTrials.gov Identifier: | NCT01289340 History of Changes |
| Other Study ID Numbers: | 6021rmc |
| Study First Received: | February 2, 2011 |
| Last Updated: | February 2, 2011 |
| Health Authority: | Israel: Ministry of Health |
Keywords provided by Rabin Medical Center:
|
wound healing pain burn |
ClinicalTrials.gov processed this record on June 18, 2013