Balance in Patients After Surgery for Torn Meniscus

The recruitment status of this study is unknown because the information has not been verified recently.
Verified November 2005 by Hadassah Medical Organization.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Hadassah Medical Organization
ClinicalTrials.gov Identifier:
NCT00256971
First received: November 20, 2005
Last updated: May 12, 2008
Last verified: November 2005
  Purpose

The important role of the menisci in knee function and in preserving knee health has been shown in several studies. Additionally to principal functions of load transmission and shock absorption, meniscus contributes to knee joint proprioception and probably also to joint stability.Study about affect of meniscus injury on balance posture has not previously been published.Surgical practice is increasingly aimed at minimal resection of injured tissue, preserving a stable meniscal remnant with as much function as possible.The purpose of this study is to determine whether menisci surgery have any effects on relatively new postural control measures, in correlation with functional balance assessment. The second purpose is to establish the affect of different types of menisci surgery on balance impairment (meniscectomy vs tear repair), in correlation with a long-term outcome.


Condition Intervention Phase
Torn Menisci
Procedure: meniscectomy
Phase 1

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Functioning Balance in Patients After Surgery for Torn Meniscus: Meniscectomy vs Meniscal Repair; A Prospective Study

Further study details as provided by Hadassah Medical Organization:

Estimated Enrollment: 150
Study Start Date: November 2005
Estimated Study Completion Date: January 2008
  Eligibility

Ages Eligible for Study:   18 Years to 40 Years
Genders Eligible for Study:   Both
Criteria

Inclusion Criteria:

  • Participants have to be healthy people
  • 18-40 years old
  • After a traumatic event of only one knee

Exclusion Criteria:

  • Previous knee surgery
  • OA per arthroscopy
  • Neurological problem
  • Any other orthopedic problem of lower limbs
  • Systemic arthritic condition (RA, SLE etc.)
  • Severe cognitive problem with restricted consent
  • Pregnancy
  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: NCT00256971

Contacts
Contact: Isabella Schwartz, MD 972-25844474 isabellas@hadassah.org.il

Locations
Israel
Hadassah Medical Organization, Recruiting
Jerusalem,, Israel
Contact: Arik , Tzukert, DMD    00 972 2 6776095    arik@hadassah.org.il   
Contact: Hadas Lemberg,, PhD    00 972 2 6777572    : lhadas@hadassah.org.il   
Principal Investigator: isabella schwartz, md         
Sponsors and Collaborators
Hadassah Medical Organization
Investigators
Principal Investigator: isabella schwartz Hadassah Medical Organization IRB
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00256971     History of Changes
Other Study ID Numbers: MEN-BM-HMO-CTIL
Study First Received: November 20, 2005
Last Updated: May 12, 2008
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration

ClinicalTrials.gov processed this record on September 16, 2014