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

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Ronald Wender, Cedars-Sinai Medical Center
ClinicalTrials.gov Identifier:
NCT01110759
First received: April 23, 2010
Last updated: October 30, 2013
Last verified: October 2013

April 23, 2010
October 30, 2013
August 2009
July 2011   (final data collection date for primary outcome measure)
postoperative pain [ Time Frame: hours to months ] [ Designated as safety issue: Yes ]
  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 ClinicalTrials.gov Archive Site
  • Nausea [ Time Frame: days to weeks ] [ Designated as safety issue: Yes ]
    1. Severity of the nausea experienced by the patient.
    2. Medication required.
    3. Time to suffer nausea.
  • Vomiting [ Time Frame: dias to weeks ] [ Designated as safety issue: Yes ]
    1. Severity
    2. Medication required
    3. Time to suffer vomiting
Not Provided
Outcomes [ Time Frame: days to weeks ] [ Designated as safety issue: Yes ]
  • 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
Observational Model: Case Control
Time Perspective: Retrospective
Not Provided
Not Provided
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 ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
200
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
Both
18 Years to 80 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01110759
Pro00019315
No
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

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP