NCT01110759

Completed

Medical Review: Hand Surgery After Local Block Versus Non-bl...

Cedars-Sinai Medical Center Source

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Other study identifiers

Sponsor study identifier

Pro00019315

Study Type

observational

Actual enrollment (reported)

200

Locations

1 country

Sites

1

Timeline

Study Start

August 2009

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

July 2011

Actual (reported)

Study Completion

July 2011

Actual (reported)

Brief Summary

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.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 200 participants
Study completion date: July 2011
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
August 2009
Date type not reported
This date has not been verified as actual or estimated.
First Submitted
April 23, 2010
Actual (reported)
First Posted
April 27, 2010
Actual (reported)
Primary Completion
July 2011
Actual (reported)
Study Completion
July 2011
Actual (reported)

Last Updated: November 1, 2013
Status Verified: October 2013
Last Update Submitted: October 30, 2013

Conditions

Carpal Tunnel Syndrome

Keywords

pain managementambulatory surgeryopioidlocal anesthesiahand surgerypostoperative pain

Outcome Measures

Primary Outcomes (1)

postoperative pain
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)
hours to months

Secondary Outcomes (2)

Nausea
days to weeks
Vomiting
dias to weeks

Other Outcomes (1)

Outcomes
days to weeks

Study Arms (2)

Under Local Infiltration

Under Peripheral Nerve Block

Eligibility Criteria

Age18 Years - 80 Years

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

Outpatients undergoing hand surgery

You may qualify if:

years old

Sponsors & Collaborators

Cedars-Sinai Medical Center
Otherlead

Study Sites (1)

Cedars Sinai Medical Center

Los Angeles, California, 90048, United States

MeSH Terms

Conditions

Carpal Tunnel SyndromeAgnosiaPain, Postoperative

Condition Hierarchy (Ancestors)

Median NeuropathyMononeuropathiesPeripheral Nervous System DiseasesNeuromuscular DiseasesNervous System DiseasesNerve Compression SyndromesCumulative Trauma DisordersSprains and StrainsWounds and InjuriesPerceptual DisordersNeurobehavioral ManifestationsNeurologic Manifestations

Study Officials

Ronald H Wender, MD
Cedars-Sinai Medical Center
PRINCIPAL INVESTIGATOR

Enrollment

200 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: CASE CONTROL
Time Perspective: RETROSPECTIVE
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Chairman, Department of Anesthesiology

Study Record Dates

First Submitted

April 23, 2010

First Posted

April 27, 2010

Study Start

August 2009

Date type not reported

This date has not been verified as actual or estimated.

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Terminated

NCT00701233

Botulinum Toxin for Carpal Tunnel Syndrome

Phase 2Withdrawn

NCT01961011

Bilateral vs Unilateral CTR

Unknown

Outpatients who underwent hand surgery under peripheral nerve block or local infiltration alone

Contact the study team to confirm eligibility.

Signs and Symptoms

Pathological Conditions, Signs and Symptoms

Postoperative Complications

Pathologic Processes

Pain

Primary Completion

July 2011

Actual (reported)

Study Completion

July 2011

Actual (reported)

Last Updated

November 1, 2013

Record last verified: 2013-10

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT01110759
Data provider: ClinicalTrials.gov
Source updated: 2013-11-01
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:38:19 UTC

Locations

US(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (2)

Other Outcomes (1)

Study Arms (2)

Under Local Infiltration

Under Peripheral Nerve Block

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

Source record

Locations