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临床试验/NCT05803096
NCT05803096已完成4 期

Self-Administered Nitrous Oxide (SANO) During Transrectal Prostate Biopsy to Reduce Patient Anxiety and Pain

Beth Israel Deaconess Medical Center1 个研究点 分布在 1 个国家目标入组 143 人开始时间: 2021年12月12日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
入组人数
143
试验地点
1
主要终点
Post-biopsy Pain (VAS-P)

研究概览

简要总结

Transrectal prostate biopsy is a commonly performed ambulatory procedure for diagnosing prostate cancer. Prostate biopsy are associated with pain or anxiety. Nitrous oxide (or laughing gas) is a well-known inhaled anesthetic which is frequently used in dental offices and for pediatric procedures to alleviate a patient's anxiety and pain. This study seeks to determine whether administration of nitrous oxide at the time of prostate biopsy will improve a patient's experience of care.

详细描述

Nitrous oxide is a well-tolerated inhaled anesthetic that has been used for decades in pediatric and adult populations and is largely viewed as effective and safe. In addition to analgesic effect, nitrous oxide also produces a dissociative euphoria and amnesia that could potentially improve patients' anxiety and experience of cancer care. When used as a single agent at concentrations ≤50%, the American Society of Anesthesiologists (ASA) classifies nitrous oxide as Minimal Sedation, producing a state in which a patient responds normally to verbal commands, maintains airway reflexes, and spontaneous ventilation. Over the past several decades nitrous oxide has become less common due to concerns of nitrous oxide environmental exposure to the care team. There are now Federal Drug Administration (FDA)-approved systems that allow patient self-administered nitrous oxide (SANO), and importantly, include a scavenger system to eliminate exhaled environmental nitrous oxide. These systems are rapidly being adopted throughout the United States in Urology practices, but to date, there have been no studies evaluating patient outcomes and possible risks with the adjunct use of SANO. This study is a prospective, randomized, controlled trial to assess patient perceived pain and anxiety related to prostate needle biopsy with or without SANO, and the frequency of complications associated with SANO. A secondary aim will be to demonstrate that the SANO at the time of prostate biopsy does not significantly increase burden on Urologist productivity, nor increase the difficulty of operator ease in performing the prostate needle biopsy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Participant, Care Provider)

盲法说明

The operating urologist and study participant will be blinded to group assignment for the duration of the study.

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Biological male
  • Aged 18 to 85 years
  • Scheduled for clinically-indicated prostate needle biopsy
  • Suitable for nitrous oxide/oxygen with willingness to be randomized to inhaled SANO or inhaled oxygen during the procedure
  • Access to an email and computer

排除标准

  • Perioral facial hair impeding good mask seal
  • Learning disabilities and/or inability to cognitively complete survey questions
  • Taken a pre-procedure benzodiazepine or narcotic.
  • Has any of the following medical conditions:
  • Inner ear, bariatric or eye surgery within the last 2 weeks,
  • Current emphysematous blebs,
  • Severe B-12 deficiency.
  • Bleomycin chemotherapy within the past year.
  • Class III or higher heart failure.
  • Undergoing novel therapy for prostate cancer

研究组 & 干预措施

Self-Administered Nitrous Oxide

Active Comparator

Patients will receive SANO in addition to periprostatic bupivacaine nerve block for the duration of prostate biopsy.

After the Urologist describes the procedure, the SANO group will have nitrous oxide turned on to 30%, ensuring that the patient is relaxed but still conversant through the procedure. The nitrous will be adjust up or down based on the patient's response to the question "are you feeling the nitrous" and "are you happy at this level". The range will be between 25 - 45%. At the end of the procedure, the SANO group will be turned down to 0% nitrous oxide, and 100% oxygen will be administered through the mask for an additional 2-3 minutes as the patient is cleaned up and repositioned to the supine position.

干预措施: Self-Administered Nitrous Oxide (Drug)

Oxygen

Placebo Comparator

Patients will receive 100% oxygen at 10 Liters/minute for the duration of prostate biopsy.

干预措施: Oxygen (Other)

结局指标

主要结局

Post-biopsy Pain (VAS-P)

时间窗: 5-minutes after prostate biopsy

Pain experienced immediately following prostate biopsy as measured by a Visual Analog Scale for Pain (VAS-P) (range: 0 \[no pain\] - 10 \[worst pain\])

Post-biopsy Anxiety (VAS-A)

时间窗: 5-minutes after prostate biopsy

Anxiety experienced immediately following prostate biopsy as measured by a Visual Analog Scale for Anxiety (VAS-A) (range: 0 \[no anxiety\] - 10 \[worst anxiety\])

Post-biopsy Anxiety Traits (STAI)

时间窗: 5-minutes after prostate biopsy

Anxious traits exhibited after prostate biopsy as measured by the State Trait Anxiety Inventory (STAI) (range: 6-36; 36 being 'worst' anxiety).

次要结局

  • Operator Assessment of "Patient Maintenance of Positioning"(Immediately after prostate biopsy; within 5 minutes after completion of biopsy.)
  • Time of Prostate Biopsy(Length of prostate biopsy; up to 30 minutes)
  • Operator Assessment of "Patient Tolerance of Procedure"(Immediately after prostate biopsy; within 5 minutes after completion of biopsy.)
  • Operator Assessment of "Tolerating Insertion of Rectal Probe"(Immediately after prostate biopsy; within 5 minutes after completion of biopsy.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Heidi Rayala

Principal Investigator

Beth Israel Deaconess Medical Center

研究点 (1)

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