Community Academic Profiles

Martin S. Angst

Effects of a peripheral nerve block on biomarkers of pain and inflammation

Contact Information

Central Contact:

Martha Tingle (650) 724-2742
Stanford University School of Medicine 300 Pasteur Drive Stanford, CA 94305

Primary Contact:

Martha Tingle (650) 724-2742
To view all clinical trials at Stanford, please see the Clinical Trials Directory.

Brief

The purpose of this study is to determine the effect of a local anesthetic nerve block on markers of inflammation and pain after a sunburn. This is important because it may provide information regarding the way that nerve blocks help with the treatment of pain and in particular provide preemptive analgesia.

Recruiting Status:

Completed

Stanford Recruiting Status:

Completed

Condition(s):

Intervention(s):

  • Procedure: femoral nerve block

Phase:

N/A

Eligibility

Ages Eligible for Study:

18 years to 50 years

Genders Eligible for Study:

Male and Female

Health of Volunteers:

People with the conditions listed in this trial can participate as controls.

Key Inclusion Criteria:

1. Between 18 and 50 years of age
2. Fluent in English language
3. Provide written informed consent
4. Skin pigmentation type II or III

Key Exclusion Criteria:

1. Current use of prescription drugs interfering with study objective
2. Use of over-the-counter analgesic/anti-inflammatory drugs within 48h of study participation
3. Current acute or chronic pain conditions
4. Significant medical conditions including psychiatric, neurological, and dermatological diseases
5. Pregnancy
6. Allergies to study drug(s)
7. Concomitant participation in other study protocol

Additional Study Details

Official Title:

Effect of peripheral nerve block on inflammatory and nociceptive biomarkers in a UV-B burn model in humans

Anticipated start date:

10/9/2007

Lead Sponsor:

Stanford University

Investigator(s):

Study Type:

Interventional

Purpose:

Prevention

Allocation:

Randomized

Masking:

Double Blind

Control:

none

Assignment:

Cross Over

Endpoints:

Efficacy

Primary Outcomes:

  • Measurement of the effect of a preemptive peripheral nerve block on the hyperalgesic response to an artificially induced sunburn.

Secondary Outcomes:

  • Measurement of the effect of a preemptive peripheral nerve block on the release of pro-inflammatory cytokines.

Total Number to be Enrolled:

15

Total Number to be Enrolled at Stanford:

15

More Information

Trial Unique Id: SU-01222008-984

Secondary ID(s):

  • eProtocol number 10740

Locations & Contacts

Stanford Locations & Contacts:

Central Contact for This Study:

Martha Tingle (650) 724-2742
Stanford University School of Medicine 300 Pasteur Drive Stanford, CA 94305

Primary Contact:

Martha Tingle (650) 724-2742

Non-Stanford Locations:

The Stanford website does not have any locations outside of Stanford listed for this trial. You may want to check clinicaltrials.gov for posible additional locations.

This listing was last updated:

11/21/2008

PLEASE NOTE:

Study Coordinators and Research Nurses cannot give medical advice over the phone. Telephone numbers are provided for obtaining additional information on specific clinical research trials only. If you have specific questions which require clinical expertise, please call your primary care physician. If you do not have a primary care physician please feel free to call the SHC Physician Referral Service at (800) 756-9000 or send an email.

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