A Pre-Operative Screening Questionnaire (AMS-Q) for Ambulatory Orthopedic Surgery Patients
1 other identifier
interventional
N/A
1 country
1
Brief Summary
We are studying whether providing patients undergoing day surgery the opportunity to have their medical history reviewed by an hospital internist before surgery leads to better results after surgery. These doctors are internal medicine specialists who are experienced in assessing patients going to surgery, making sure they are "fine-tuned" before their operation. We believe this will ensure the safest and best surgical outcomes. The study involves the patient filling out a 3 page questionnaire for review by the internist prior to surgery. Additionally, patients will receive a follow-up phone call one week after surgery asking about the experience at the hospital and a questionnaire in the mail three months later to see if the patient had any medical problems after leaving the hospital.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Dec 2005
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2005
CompletedFirst Submitted
Initial submission to the registry
June 14, 2006
CompletedFirst Posted
Study publicly available on registry
June 16, 2006
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2007
CompletedMarch 13, 2017
March 1, 2017
June 14, 2006
March 9, 2017
Conditions
Keywords
Interventions
Eligibility Criteria
You may qualify if:
- All patients having ambulatory surgery performed by one of our participating surgeons during the study period.
You may not qualify if:
- Patients who speak neither English nor Spanish.
- Patients who have had any surgery in the previous 6 months.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hospital for Special Surgery
New York, New York, 10021, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Lisa A Mandl, MD MPH
Hospital for Special Surgery, New York
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
June 14, 2006
First Posted
June 16, 2006
Study Start
December 1, 2005
Study Completion
June 1, 2007
Last Updated
March 13, 2017
Record last verified: 2017-03