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临床试验/NCT07824258
NCT07824258招募中1 期

A Randomized Controlled Trial of Post-vasectomy Pain Management

Columbia University2 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2026年9月10日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
招募中
入组人数
200
试验地点
2
主要终点
Brief Pain Inventory (BPI) - Total Score

研究概览

简要总结

This is a prospective four-armed unblinded randomized controlled trial to assess four different potential post-operative treatment options for men who undergo a vasectomy. The aims of this study are:

  • To determine whether the addition of nonsteroidal anti-inflammatory drugs (NSAIDs) to acetaminophen results in improved pain after vasectomy;
  • To determine whether the addition of opioid pain medication to acetaminophen and/or NSAIDs results in improved pain after vasectomy;
  • To determine whether the use of NSAIDs for post-operative pain management increases risk of hematoma after vasectomy.

详细描述

The purpose of this study is to evaluate and compare commonly used post-vasectomy pain regimens. Eligible participants will be adult male patients who elect to undergo vasectomy with a urologist at Columbia University Medical Center with no history of kidney or liver disease, chronic pain conditions, or drug abuse. Prospectively enrolled participants will be randomized to one of four study arms, which will differ by post-operative pain regimens as follows:

  • Arm 1: 975 mg acetaminophen every 6 hours for the first 48 hours to a maximum of 7 days;
  • Arm 2: 975 mg acetaminophen and 600 mg ibuprofen every 6 hours for the first 48 hours to a maximum of 7 days;
  • Arm 3: 975 mg acetaminophen every 6 hours for the first 48 hours to a maximum of 7 days with a prescription for 6 tablets of 5 mg oxycodone every 6 hours as needed;
  • Arm 4: 975 mg acetaminophen and 600 mg ibuprofen every 6 hours for the first 48 hours to a maximum of 7 days with a prescription for 6 tablets of 5 mg oxycodone every 6 hours as needed.

Other than the differing pain regimens, all treatment and pre- and post-operative counselling will be standard of care at the discretion of the treating urologists. Participants will be contacted at 1 day and 7 days post-operatively to complete Brief Pain Inventory (BPI) questionnaires, assess how many tablets of oxycodone they have taken, and assess whether they would be comfortable returning to work. At post-operative visits, their treating urologist will assess them for the presence of hematoma. Comparisons will be made between study arms to assess for differences.

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
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • - Consent for vasectomy

排除标准

  • History of kidney or liver disease
  • History of chronic pain condition
  • History of drug abuse

研究组 & 干预措施

Acetaminophen only

Experimental

Participants are encouraged to take only acetaminophen 975 mg every 6 hours for the first 48 hours to a maximum of 7 days after surgery.

干预措施: Acetaminophen (Drug)

Acetaminophen + oxycodone

Experimental

Participants are encouraged to take acetaminophen 975 mg every 6 hours for the first 48 hours to a maximum of 7 days after surgery, and a prescription for 6 tablets of oxycodone 5 mg will be prescribed to take every 6 hours as needed for pain.

干预措施: Acetaminophen (Drug)

Acetaminophen + ibuprofen

Experimental

Participants are encouraged to take acetaminophen 975 mg and ibuprofen 600 mg every 6 hours for the first 48 hours to a maximum 7 days after surgery.

干预措施: Acetaminophen (Drug)

Acetaminophen + ibuprofen

Experimental

Participants are encouraged to take acetaminophen 975 mg and ibuprofen 600 mg every 6 hours for the first 48 hours to a maximum 7 days after surgery.

干预措施: ibuprofen (Drug)

Acetaminophen + ibuprofen + oxycodone

Experimental

Participants are encouraged to take acetaminophen 976 mg and ibuprofen 600 mg every 6 hours for the first 48 hours to a maximum of 7 days after surgery, and a prescription for 6 tablets of oxycodone 5 mg will be prescribed to take every 6 hours as needed for pain.

干预措施: ibuprofen (Drug)

Acetaminophen + oxycodone

Experimental

Participants are encouraged to take acetaminophen 975 mg every 6 hours for the first 48 hours to a maximum of 7 days after surgery, and a prescription for 6 tablets of oxycodone 5 mg will be prescribed to take every 6 hours as needed for pain.

干预措施: oxycodone (Drug)

Acetaminophen + ibuprofen + oxycodone

Experimental

Participants are encouraged to take acetaminophen 976 mg and ibuprofen 600 mg every 6 hours for the first 48 hours to a maximum of 7 days after surgery, and a prescription for 6 tablets of oxycodone 5 mg will be prescribed to take every 6 hours as needed for pain.

干预措施: Acetaminophen (Drug)

Acetaminophen + ibuprofen + oxycodone

Experimental

Participants are encouraged to take acetaminophen 976 mg and ibuprofen 600 mg every 6 hours for the first 48 hours to a maximum of 7 days after surgery, and a prescription for 6 tablets of oxycodone 5 mg will be prescribed to take every 6 hours as needed for pain.

干预措施: oxycodone (Drug)

结局指标

主要结局

Brief Pain Inventory (BPI) - Total Score

时间窗: 1 to 7 days post operatively

The Brief Pain Inventory is a self-reported questionnaire to assess pain. Final scores will be averaged. The score range is 0 to 10, where a higher score indicates a worse outcome.

次要结局

  • Brief Pain Inventory (BPI) - Pain Interference Score(1 to 7 days post operatively)
  • Brief Pain Inventory (BPI) - Pain Severity Score(1 to 7 days post operatively)

研究者

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

Aaron Brant

Assistant Professor of Urology

Columbia University

研究点 (2)

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