Medical Review: Hand Surgery After Local Block Versus Non-block

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. Identifier: NCT01110759
Recruitment Status : Completed
First Posted : April 27, 2010
Last Update Posted : November 1, 2013
Information provided by (Responsible Party):
Ronald Wender, Cedars-Sinai Medical Center

April 23, 2010
April 27, 2010
November 1, 2013
August 2009
July 2011   (Final data collection date for primary outcome measure)
postoperative pain [ Time Frame: hours to months ]
  1. Severity of the pain experienced before patient left the surgery center and after patient arrived at home
  2. Pain medication (amounts of opioids and non opioids pills) required

d)Time to suffer pain at the surgical site (hand) (days, weeks, or months)

Not Provided
Complete list of historical versions of study NCT01110759 on Archive Site
  • Nausea [ Time Frame: days to weeks ]
    1. Severity of the nausea experienced by the patient.
    2. Medication required.
    3. Time to suffer nausea.
  • Vomiting [ Time Frame: dias to weeks ]
    1. Severity
    2. Medication required
    3. Time to suffer vomiting
Not Provided
Outcomes [ Time Frame: days to weeks ]
  • Presence of any other problems: (e.g., headaches, dizziness, drowsiness, fatigue, constipation, difficulty voiding.)
  • Time taken to return to normal activities after surgery
  • Satisfaction with the pain management after surgery
Not Provided
Medical Review: Hand Surgery After Local Block Versus Non-block
Retrospective Chart-review Study Involving Outpatients Who Underwent Hand Surgery With Local Anesthesia: Comparing Outcome With a Peripheral Nerve Block vs. Local Infiltration Alone
In this study, the effects of local block vs non block will be assessed with respect to postoperative outcomes (such as pain score, and recovery profiles) in outpatients after hand surgery.
Analyzing medical records and through a telephone questionnaire, in a retrospective and prospective review respectively.
Observational Model: Case Control
Time Perspective: Retrospective
Not Provided
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Non-Probability Sample
Outpatients undergoing hand surgery
Carpal Tunnel Syndrome
Not Provided
  • Under Local Infiltration
  • Under Peripheral Nerve Block
Not Provided

*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
Same as current
July 2011
July 2011   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • 18-80 years old
  • Outpatients who underwent hand surgery under peripheral nerve block or local infiltration alone

Exclusion Criteria:

  • Patients who do not meet inclusion criteria
Sexes Eligible for Study: All
18 Years to 80 Years   (Adult, Senior)
Contact information is only displayed when the study is recruiting subjects
United States
Not Provided
Not Provided
Ronald Wender, Cedars-Sinai Medical Center
Cedars-Sinai Medical Center
Not Provided
Principal Investigator: Ronald H Wender, MD Cedars-Sinai Medical Center
Cedars-Sinai Medical Center
October 2013