Now Available: Final Rule for FDAAA 801 and NIH Policy on Clinical Trial Reporting

Cronic Pressure Wounds and Relation With Gender (preswound)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified November 2010 by SB Istanbul Education and Research Hospital.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
SB Istanbul Education and Research Hospital
ClinicalTrials.gov Identifier:
NCT01347489
First received: May 3, 2011
Last updated: May 4, 2011
Last verified: November 2010
  Purpose
There is no exact scientfic data about gender relationship with cronic pressure wounds (CPW). This research is aimed first to reveal gender relationship with CPW and aimed secondarily to reveal the gender related couse(es).

Condition
Wound

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Cronic Pressure Wounds and Relation With Gender

Resource links provided by NLM:


Further study details as provided by SB Istanbul Education and Research Hospital:

Estimated Enrollment: 2
Study Start Date: November 2010
Estimated Study Completion Date: December 2012
Estimated Primary Completion Date: June 2011 (Final data collection date for primary outcome measure)
Detailed Description:
There is no exact scientific data about gender relationship with cronic pressure wounds (CPW). Researches about this subject is generally related to prevention and management of the process. But gender difference is not exactly researched in the literature. This research is aimed first to reveal gender relationship with CPW and aimed secondarily to reveal the gender related couse(es).
  Eligibility

Ages Eligible for Study:   17 Years to 90 Years   (Child, Adult, Senior)
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Cronic pressure wound patients
Criteria

Inclusion Criteria:

  • Cronic pressure wound patients

Exclusion Criteria:

  • Operated cronic pressure wounds
  Contacts and Locations
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01347489

Locations
Turkey
Bezmialem Vakif University Recruiting
Istanbul, Turkey
Contact: adnan yuksel, prof.    +902124531700    ayuksel@bezmialem.edu.tr   
Sponsors and Collaborators
SB Istanbul Education and Research Hospital
Investigators
Principal Investigator: erhan aysan, Assoc. Prof. Bezmialem Vakif University
  More Information

Responsible Party: Erhan Aysan, Assoc. Prof.
ClinicalTrials.gov Identifier: NCT01347489     History of Changes
Other Study ID Numbers: 3-Aysan 
Study First Received: May 3, 2011
Last Updated: May 4, 2011
Health Authority: Turkey: Ministry of Health

Keywords provided by SB Istanbul Education and Research Hospital:
gender

Additional relevant MeSH terms:
Wounds and Injuries

ClinicalTrials.gov processed this record on September 30, 2016