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

Primary Purpose

Prostate Disease, Malignancy, Benign Prostatic Hyperplasia

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Self-Administered Nitrous Oxide
Oxygen
Sponsored by
Beth Israel Deaconess Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Prostate Disease focused on measuring prostate biopsy, nitrous oxide, prostate cancer, ambulatory, patient experience of care

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria: 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 Exclusion Criteria: 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

Sites / Locations

  • Beth Israel Deaconess Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Self-Administered Nitrous Oxide

Oxygen

Arm Description

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.

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

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Time of prostate biopsy
Length of procedure will be compared between arms to assess whether SANO significantly lengthens prostate biopsy
Operator ease of performing procedure
Operating urologist will be asked to fill out a three-item "operator survey" that asks if "Insertion of rectal probe," "patient maintenance of positioning," and "patient tolerance of procedure," was "worse than expected (-1)", "as expected (0)" or "better than expected (+1)" the composite score will be compared between groups

Full Information

First Posted
February 28, 2023
Last Updated
March 25, 2023
Sponsor
Beth Israel Deaconess Medical Center
Collaborators
Brigham and Women's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05803096
Brief Title
Self-Administered Nitrous Oxide (SANO) During Transrectal Prostate Biopsy to Reduce Patient Anxiety and Pain
Official Title
Self-Administered Nitrous Oxide (SANO) During Transrectal Prostate Biopsy to Reduce Patient Anxiety and Pain
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
December 12, 2021 (Actual)
Primary Completion Date
September 2, 2022 (Actual)
Study Completion Date
September 9, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beth Israel Deaconess Medical Center
Collaborators
Brigham and Women's Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Disease, Malignancy, Benign Prostatic Hyperplasia, Prostate Cancer, Prostate Adenocarcinoma, Anxiety and Fear, Pain
Keywords
prostate biopsy, nitrous oxide, prostate cancer, ambulatory, patient experience of care

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Subjects will be randomized 1:1 to either SANO (treatment) or oxygen (placebo control) after completion of baseline assessment. The results of the randomization will not be disclosed to patients as part of the study (patient-blinded).
Masking
ParticipantCare Provider
Masking Description
The operating urologist and study participant will be blinded to group assignment for the duration of the study.
Allocation
Randomized
Enrollment
128 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Self-Administered Nitrous Oxide
Arm Type
Active Comparator
Arm Description
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.
Arm Title
Oxygen
Arm Type
Placebo Comparator
Arm Description
Patients will receive 100% oxygen at 10 Liters/minute for the duration of prostate biopsy.
Intervention Type
Drug
Intervention Name(s)
Self-Administered Nitrous Oxide
Other Intervention Name(s)
nitrous oxide
Intervention Description
Nitrous oxide administered at concentrations of mild sedation (20-45%) for the duration of prostate biopsy.
Intervention Type
Other
Intervention Name(s)
Oxygen
Intervention Description
Oxygen will be administered at 10 Liters/min for the duration of prostate biopsy.
Primary Outcome Measure Information:
Title
Post-biopsy pain (VAS-P)
Description
Pain experienced immediately following prostate biopsy as measured by a Visual Analog Scale for Pain (VAS-P) (range: 0 [no pain] - 10 [worst pain])
Time Frame
5-minutes after prostate biopsy
Title
Post-biopsy anxiety (VAS-A)
Description
Anxiety experienced immediately following prostate biopsy as measured by a Visual Analog Scale for Anxiety (VAS-A) (range: 0 [no anxiety] - 10 [worst anxiety])
Time Frame
5-minutes after prostate biopsy
Title
Post-biopsy anxiety traits (STAI)
Description
Anxious traits exhibited after prostate biopsy as measured by the State Trait Anxiety Inventory (STAI) (range: 6-36; 36 being 'worst' anxiety).
Time Frame
5-minutes after prostate biopsy
Secondary Outcome Measure Information:
Title
Time of prostate biopsy
Description
Length of procedure will be compared between arms to assess whether SANO significantly lengthens prostate biopsy
Time Frame
Length of prostate biopsy; up to 30 minutes
Title
Operator ease of performing procedure
Description
Operating urologist will be asked to fill out a three-item "operator survey" that asks if "Insertion of rectal probe," "patient maintenance of positioning," and "patient tolerance of procedure," was "worse than expected (-1)", "as expected (0)" or "better than expected (+1)" the composite score will be compared between groups
Time Frame
Immediately after prostate biopsy

10. Eligibility

Sex
Male
Gender Based
Yes
Gender Eligibility Description
Participants with a prostate may be eligible for the study.
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 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 Exclusion Criteria: 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Heidi Rayala, MD, PhD
Organizational Affiliation
Beth Israel Deaconess Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beth Israel Deaconess Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
IPD is not intended to be shared to personnel outside of pre-defined research staff.
Citations:
PubMed Identifier
21944136
Citation
Loeb S, Carter HB, Berndt SI, Ricker W, Schaeffer EM. Complications after prostate biopsy: data from SEER-Medicare. J Urol. 2011 Nov;186(5):1830-4. doi: 10.1016/j.juro.2011.06.057. Epub 2011 Sep 23.
Results Reference
background
PubMed Identifier
22232535
Citation
Rosario DJ, Lane JA, Metcalfe C, Donovan JL, Doble A, Goodwin L, Davis M, Catto JW, Avery K, Neal DE, Hamdy FC. Short term outcomes of prostate biopsy in men tested for cancer by prostate specific antigen: prospective evaluation within ProtecT study. BMJ. 2012 Jan 9;344:d7894. doi: 10.1136/bmj.d7894.
Results Reference
background
PubMed Identifier
1819967
Citation
Jastak JT, Donaldson D. Nitrous oxide. Anesth Prog. 1991 Jul-Oct;38(4-5):142-53. No abstract available.
Results Reference
background
PubMed Identifier
29334501
Citation
Practice Guidelines for Moderate Procedural Sedation and Analgesia 2018: A Report by the American Society of Anesthesiologists Task Force on Moderate Procedural Sedation and Analgesia, the American Association of Oral and Maxillofacial Surgeons, American College of Radiology, American Dental Association, American Society of Dentist Anesthesiologists, and Society of Interventional Radiology. Anesthesiology. 2018 Mar;128(3):437-479. doi: 10.1097/ALN.0000000000002043. No abstract available.
Results Reference
background

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

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