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A Pre-Operative Screening Questionnaire (AMS-Q) for Ambulatory Orthopedic Surgery Patients

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00337584
First Posted: June 16, 2006
Last Update Posted: March 13, 2017
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:
Hospital for Special Surgery, New York
  Purpose
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.

Condition Intervention
Ambulatory Surgery Procedure: Pre-surgical screening

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)

Further study details as provided by Hospital for Special Surgery, New York:

Study Start Date: December 2005
Study Completion Date: June 2007
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Criteria

Inclusion Criteria:

  • All patients having ambulatory surgery performed by one of our participating surgeons during the study period.

Exclusion Criteria:

  • Patients who speak neither English nor Spanish.
  • Patients who have had any surgery in the previous 6 months.
  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): NCT00337584


Locations
United States, New York
Hospital for Special Surgery
New York, New York, United States, 10021
Sponsors and Collaborators
Hospital for Special Surgery, New York
Investigators
Principal Investigator: Lisa A Mandl, MD MPH Hospital for Special Surgery, New York
  More Information

ClinicalTrials.gov Identifier: NCT00337584     History of Changes
Other Study ID Numbers: 24003
First Submitted: June 14, 2006
First Posted: June 16, 2006
Last Update Posted: March 13, 2017
Last Verified: March 2017

Keywords provided by Hospital for Special Surgery, New York:
out patient surgery
quality improvement