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OpenTrials
Completed

NCT Number: NCT00456872

Contrast of Buffered Vs. Unbuffered Lidocaine in Bone Marrow Biopsies

Oncology patients require numerous invasive procedures throughout their disease process including bone marrow biopsies (BMB). BMB.s are performed by a significant number of health care providers. One of the biggest concerns for health care providers is to improve patient comfort. The goal of this study was to reduce pain during BMBs.

Specific aims of the study were to determine if there is a difference in patients' perceived pain during injection of the pre-procedure anesthetic when buffered versus unbuffered lidocaine is administered to patient's receiving bone marrow biopsies.

A double blind, experimental crossover design was used to examine the difference in pain levels when using buffered versus unbuffered lidocaine prior to the bilateral bone marrow biopsy procedure. Based on a power analysis for a paired t-test, a convenience sample of 48 patients was enrolled into the study. Patients served as their own control. The site of first biopsy, and which lidocaine solution was administered first, were randomized. A 100mm visual analogue scale (VAS) was used to measure pain.

All data has been collected, are currently under analysis, and results will be completed in August 2006. Differences in groups will be examined using a paired t-test. A demographic questionnaire was used to gather select demographic variables. Correlative studies will be done to examine the relationship between the patient's perceived pain scores and several exploratory variables. Results of this study may change the current type of anesthetic used pre-BMBs thus improving patient comfort.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Ohio State University James Cancer Hospital

Columbus, Ohio, 43210, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Any newly diagnosed patient at the Arthur G. James Cancer Hospital and Richard J. Solove Research Institute whose Hematologist or Oncologist has ordered them to undergo a bilateral bone marrow biopsy for diagnostic and /or treatment purposes.
  • 18 years of age or older.

Exclusion criteria

  • Pregnant or Lactating women.
  • Patients with allergies to local anesthetics.
  • Patients requiring a unilateral bone marrow biopsy.
  • Patients that cannot lie flat in either the supine or prone position.
  • Patients that have used any of the following: narcotics, non-narcotic analgesia or an anti-anxiolytic medication on the same calendar day as the scheduled procedure. These medications will not be given to the participant at any time before or during the procedure.
  • Patients on long-acting narcotic medication.
  • Patients with neuropathy in the posterior iliac crest area
  • Patients with a platelet count less than 20,000.
  • Patients who are cognitively impaired or unable to self-report pain using the VAS.
  • Patients with known bone metastasis.

Treatment and study plan

Lidocaine

Drug

Other names: Xylocaine, lignocaine

Primary outcomes

  1. Difference in patients perceived pain during injection of the pre-procedure anesthetic

    Time frame: Up to 24 months

    Determine difference in patients perceived pain during injection of pre-procedure anesthetic when buffered versus unbuffered lidocaine is administered.

Secondary outcomes

  1. Change in pain level over time after anesthetic is administered.

    Time frame: Up to 24 months

    Determine if pain levels change over time after anesthetic is administered.

  2. Investigate relationships between patients perceived pain scores and variables.

    Time frame: Up to 24 months

    Variables include gender, ethnicity, stage and extent of disease, body mass index, history of pain tolerance, and perceived emotional support.

Sponsors and collaborators

Lead sponsor

Ohio State University Comprehensive Cancer Center

Other

Registry information

Official study title

A Contrast of Buffered Vs. Unbuffered Lidocaine in Bone Marrow Biopsies

Important dates

Study start
2004
Primary completion
2006
Study completion
2007
First posted
Apr 5, 2007
Registry last updated
Apr 4, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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