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Assessment of the Effect of Age on Duration of Analgesia From Single-shot Femoral Nerve Blocks

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University of Washington

Status

Unknown

Conditions

Analgesia

Study type

Observational

Funder types

Other

Identifiers

NCT04495413
STUDY00008754

Details and patient eligibility

About

Cohort study to examine the effect of age on duration of analgesia in patients receiving single-shot femoral nerve block prior to surgery, by postoperative phone follow-up questionnaire.

Full description

The purpose of this study is to find out how differences in age can affect the duration of pain relief from a femoral nerve block. Complete recovery after leg surgery involves healing of tissues at the surgical site, recovery of muscle strength and range-of-motion. Some pain is normally experienced after leg surgery. At the hospital, pain is usually treated with pain medicines, and/or a nerve block procedure. A nerve block involves injecting a local anesthetic beside the nerves to numb the nerves that supply feeling to the knee joint and surrounding tissues. The choice as to whether a participant has a nerve block or not is made by the participant and their surgeon and is not determined by this research study. The study aim is to find out how long a nerve block can relieve postsurgical pain, and whether that duration is affected by the age of the participant.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adult patients (age >18 years)
  • American Society of Anesthesiology physical status 1-3
  • Having ambulatory surgery, who have received a single-shot femoral nerve block
  • Able to read and understand English
  • Have access to a phone after surgery

Exclusion criteria

  • Pediatric patients (age <18 years)
  • American Society of Anesthesiology physical status >3
  • Unable to read and understand English
  • Unable to have access to a phone after surgery

Trial contacts and locations

1

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Central trial contact

Adam J Claessens, DO

Data sourced from clinicaltrials.gov

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