跳至主要内容
临床试验/NCT06215859
NCT06215859
已完成
3 期

Multi-Center, Randomized, Double-Blind, Placebo (Double-Dummy) and Active-Controlled, Parallel-Group Study of MR-107A-02 for the Treatment of Acute Postoperative Pain Following Herniorrhaphy

Viatris Specialty LLC18 个研究点 分布在 1 个国家目标入组 579 人2023年12月29日

概览

阶段
3 期
干预措施
MR-107A-02
疾病 / 适应症
Acute Pain
发起方
Viatris Specialty LLC
入组人数
579
试验地点
18
主要终点
Summed Pain Intensity Difference (SPID) for MR-107A-02 versus placebo.
状态
已完成
最后更新
2个月前

概览

简要总结

MR-107A-02 is being studied to investigate its efficacy and safety for treatment of acute pain after herniorrhaphy.

注册库
clinicaltrials.gov
开始日期
2023年12月29日
结束日期
2025年3月12日
最后更新
2个月前
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

责任方
Sponsor

入排标准

入选标准

  • Main Inclusion Criteria:
  • 1\. Requirement for unilateral open inguinal herniorrhaphy with mesh under general anesthesia.
  • 3\. Has an American Society of Anesthesiologists Physical Status of I, II, or III.
  • 4\. Pain Intensity (PI) using NRS-R ≥4 at any given timepoint during the 5 hours following end of surgery in the eligibility assessment as well as in the baseline assessment (NRS-R and NRS-A) immediately pre-dosing.
  • 5\. Rating of moderate or severe pain on a 4-point categorical pain rating scale (i.e., none, mild, moderate, severe) during the 5 hours following end of surgery.
  • 6\. Able to understand and complete the study requirements (including literacy, to enable diary and questionnaire completion), provide written informed consent, and agree to abide by the study protocol and its restrictions.

排除标准

  • Previously dosed with this formulation of MR 107A
  • Had any prior inguinal hernia repair in the past 24 months.
  • Has a planned concurrent surgical procedure (e.g., bilateral herniorrhaphy).
  • Has a pre-existing concurrent acute or chronic painful physical/restrictive condition expected to require analgesic treatment in the postoperative period for pain that is not strictly related to the herniorrhaphy, and which may confound the postoperative assessments.
  • Known hypersensitivity to aspirin, NSAIDs, or other medication used in the study.
  • Body mass index (BMI) \>40 kg/m2 at screening.
  • Body weight of \<43 kg (105.8 lbs) at screening.
  • History of GI bleeding or peptic ulcer disease.
  • Known active inflammatory bowel disease, e.g., Crohn's Disease or ulcerative colitis.
  • A history of bleeding disorders that may affect coagulation.

研究组 & 干预措施

MR-107A-02

15 mg Twice daily (BID) during in patient phase (0-48 hours following randomization) 15 mg BID dosing morning and evening, during out patient phase (5 days) .

干预措施: MR-107A-02

Tramadol

50 mg, administered every 6 hours (q6h) during the in patient phase (0-48 hours following randomization). Placebo will be administered during out patient phase.

干预措施: Tramadol

Tramadol

50 mg, administered every 6 hours (q6h) during the in patient phase (0-48 hours following randomization). Placebo will be administered during out patient phase.

干预措施: Placebo

Placebo

Placebo is administered every 6 hours (q6h) during the in patient phase (0-48 hours following randomization) and twice daily during the out patient phase.

干预措施: Placebo

MR-107A-02

15 mg Twice daily (BID) during in patient phase (0-48 hours following randomization) 15 mg BID dosing morning and evening, during out patient phase (5 days) .

干预措施: Herniorrhaphy

Tramadol

50 mg, administered every 6 hours (q6h) during the in patient phase (0-48 hours following randomization). Placebo will be administered during out patient phase.

干预措施: Herniorrhaphy

Placebo

Placebo is administered every 6 hours (q6h) during the in patient phase (0-48 hours following randomization) and twice daily during the out patient phase.

干预措施: Herniorrhaphy

结局指标

主要结局

Summed Pain Intensity Difference (SPID) for MR-107A-02 versus placebo.

时间窗: 48 hours after randomization

SPID based on a 0 to 10-point numeric rating scale with activity (NRS-A) for MR-107A-02 versus placebo.

次要结局

  • Number of doses of opioid rescue medication taken for MR-107A-02 versus placebo.(7 days after randomization)
  • Summed Pain Intensity Difference (SPID) for MR-107A-02 versus tramadol(48 hours after randomization)
  • Proportion of subjects using no opioid rescue medication MR-107A-02 versus placebo.(7 days after randomization)
  • Summed Pain Intensity Difference (SPID) for tramadol versus placebo.(7 days after randomization)

研究点 (18)

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