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临床试验/NCT03090152
NCT03090152已完成4 期

Minimal Opioid Use After Total Hip Replacement (THR): a Blinded Randomized Placebo-controlled Study

Hospital for Special Surgery, New York1 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2017年3月8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
发起方
入组人数
180
试验地点
1
主要终点
Opioid Use

研究概览

简要总结

Total hip arthroplasty can be associated with significant postoperative pain. Side effects of pain management may impair participation in physical therapy and slow readiness for discharge from the hospital. In a previous study done by the investigators' group, epidural patient controlled analgesia (EPCA) with a hydromorphone containing solution appeared to have a more favorable pain profile with ambulation, but greater side effects compared to injection of a peri-articular cocktail. The use of opioid was greater in the peri-articular injection group (PAI). There was no difference in length of stay. In view of the controversy over opioid use, the investigators would like to develop an optimal opioid sparing pain management approach by comparing 3 different protocols 1) Plain local anesthetic EPCA; 2) PAI; 3) EPCA + PAI; all in conjunction with a multimodal opioid sparing pain regimen. The goal would be to maximize pain control while minimizing opioid use and side-effects.

详细描述

Long acting narcotics or scheduled doses of narcotics are often used as part of a multimodal pain regimen. In this study, this is eliminated. Instead, it uses a cocktail of different drugs including intraoperative Ketamine use (NMDA receptor antagonist), intra-op Benadryl (to decrease excitation of nociceptors) and IV Tylenol. The narcotic free regimen starts preoperatively with the use of Aspirin,Clonidine patch, Cymbalta (Duloxetine), and is maintained both intraoperatively and post operatively. Baby ASA (81mg) is being used as an anti-inflammatory agent. A number of studies including the one by Morris et al. (2009), have shown via in vitro experiments that low dose aspirin decreases polymorphonuclear leukocyte and macrophage accumulation. It inhibits thromboxane making it an antithrombotic agent as well. The concern with aspirin has been major bleeding. Several studies in the orthopedic patient population using ≤81 mg of aspirin have shown that it does not increase bleeding (Cuellar, Mantz). At HSS, patients are routinely continued on baby aspirin when needed for its cardio protective effect. Devereaux in the POISE trial did show an increased risk of bleeding when ASA was given preoperatively at a dose of 200 mg. In our study, all patients will be given intravenous tranexamic acid which should mitigate against the risk of bleeding. Duloxetine is also being added. In a recent study done at HSS. Duloxetine was found to decrease the amount of opioid use and nausea. If found to be more effective with the use of EPCA vs. PAI or combination of the two, a new way of managing postop pain while minimizing Nnartcuoreti co fu Ssetu adsy per CDC recommendation will be helpful in managing patients post-operatively.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
50 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Any patient with osteoarthritis scheduled for primary total hip arthroplasty with a participating surgeon
  • Planned use of regional anesthesia
  • Planned posterolateral surgical approach
  • Age Range 45-80
  • Ability to follow study protocol

排除标准

  • Any patient with age <45 or >80
  • Any patient with planned anterior surgical approach
  • Any patient with prior major ipsilateral hip surgery
  • Any patient intending to receive general anesthesia
  • Any patient with an ASA of IV
  • Any patient with insulin-dependent diabetes
  • Any patient with hepatic (liver) failure (history of cirrhosis or elevated LFT's)
  • Any patient with chronic renal (kidney) failure (formal diagnosis of renal disease of elevated creatinine)
  • Any patient with history of gastric (stomach) ulcer
  • Chronic opioid use (taking opioids for >3 mo duration on a daily basis)
  • Chronic analgesic use (i.e. lyrica, gabapentin) for >3 mo duration
  • Stress dose steroids
  • Use of antidepressants
  • Contraindications to aspirin
  • Allergy to any of the medications (or adhesives) involved in the study protocol
  • Non-English speakers.

研究组 & 干预措施

Periarticular Injection (PAI)

Active Comparator
  • Aspirin and nerve pain medications including duloxetine and clonidine patch prior to surgery.
  • Peri-articular injection in the operating room
  • Combined Spinal Epidural with 1.5% Mepivacaine 4cc
  • A pain regimen while in the hospital that includes EPCA (saline) Duloxetine (Cymbalta) - by mouth Ketorolac (Toradol) - IV Celecoxib (Celebrex) - by mouth Acetaminophen (Tylenol) - IV
  • Acetaminophen and celecoxib for pain control once out of the hospital. Patients will also receive a prescription for an opioid medication in case they need it.

干预措施: Periarticular injection (Deep injection) (Procedure)

Periarticular Injection (PAI)

Active Comparator
  • Aspirin and nerve pain medications including duloxetine and clonidine patch prior to surgery.
  • Peri-articular injection in the operating room
  • Combined Spinal Epidural with 1.5% Mepivacaine 4cc
  • A pain regimen while in the hospital that includes EPCA (saline) Duloxetine (Cymbalta) - by mouth Ketorolac (Toradol) - IV Celecoxib (Celebrex) - by mouth Acetaminophen (Tylenol) - IV
  • Acetaminophen and celecoxib for pain control once out of the hospital. Patients will also receive a prescription for an opioid medication in case they need it.

干预措施: Periarticular injection (Superficial injection) (Procedure)

Periarticular Injection (PAI)

Active Comparator
  • Aspirin and nerve pain medications including duloxetine and clonidine patch prior to surgery.
  • Peri-articular injection in the operating room
  • Combined Spinal Epidural with 1.5% Mepivacaine 4cc
  • A pain regimen while in the hospital that includes EPCA (saline) Duloxetine (Cymbalta) - by mouth Ketorolac (Toradol) - IV Celecoxib (Celebrex) - by mouth Acetaminophen (Tylenol) - IV
  • Acetaminophen and celecoxib for pain control once out of the hospital. Patients will also receive a prescription for an opioid medication in case they need it.

干预措施: Placebo (Drug)

Epidural Patient-Controlled Analg (EPCA)

Active Comparator
  • Aspirin and nerve pain medications including duloxetine and clonidine patch prior to surgery.
  • Combined Spinal Epidural with 1.5% Mepivacaine 4cc
  • A pain regimen while in the hospital that consists of Epidural PCA (EPCA) with 0.06% bupivacaine. Duloxetine (Cymbalta) - by mouth Ketorolac (Toradol) - IV Celecoxib (Celebrex) - by mouth Acetaminophen (Tylenol) - IV The EPCA will be removed when pain is well-controlled. Other medications, including opioids, will be available.
  • Acetaminophen and celecoxib for pain control once out of the hospital. Patients will also receive a prescription for an opioid medication in case they need it.

干预措施: Bupivacaine (Drug)

PAI + EPCA

Experimental
  • Aspirin and nerve pain medications including duloxetine and clonidine
  • Combined Spinal Epidural with 1.5% Mepivacaine 4cc
  • Anesthetic, Antiemetic and peri-articular injection in the operating room
  • A pain regimen while in the hospital that consists of EPCA (with 0.06% bupivacaine) Duloxetine (Cymbalta) - by mouth Ketorolac (Toradol) - IV Celecoxib (Celebrex) - by mouth Acetaminophen (Tylenol) - IV The EPCA will be removed when pain is well-controlled. Other medications, including opioids, will be available.
  • Acetaminophen and celecoxib for pain control once out of the hospital. Patients will also receive a prescription for an opioid medication in case they need it.

干预措施: Periarticular injection (Deep injection) (Procedure)

PAI + EPCA

Experimental
  • Aspirin and nerve pain medications including duloxetine and clonidine
  • Combined Spinal Epidural with 1.5% Mepivacaine 4cc
  • Anesthetic, Antiemetic and peri-articular injection in the operating room
  • A pain regimen while in the hospital that consists of EPCA (with 0.06% bupivacaine) Duloxetine (Cymbalta) - by mouth Ketorolac (Toradol) - IV Celecoxib (Celebrex) - by mouth Acetaminophen (Tylenol) - IV The EPCA will be removed when pain is well-controlled. Other medications, including opioids, will be available.
  • Acetaminophen and celecoxib for pain control once out of the hospital. Patients will also receive a prescription for an opioid medication in case they need it.

干预措施: Periarticular injection (Superficial injection) (Procedure)

PAI + EPCA

Experimental
  • Aspirin and nerve pain medications including duloxetine and clonidine
  • Combined Spinal Epidural with 1.5% Mepivacaine 4cc
  • Anesthetic, Antiemetic and peri-articular injection in the operating room
  • A pain regimen while in the hospital that consists of EPCA (with 0.06% bupivacaine) Duloxetine (Cymbalta) - by mouth Ketorolac (Toradol) - IV Celecoxib (Celebrex) - by mouth Acetaminophen (Tylenol) - IV The EPCA will be removed when pain is well-controlled. Other medications, including opioids, will be available.
  • Acetaminophen and celecoxib for pain control once out of the hospital. Patients will also receive a prescription for an opioid medication in case they need it.

干预措施: Bupivacaine (Drug)

结局指标

主要结局

Opioid Use

时间窗: within 24 hours after surgery

Oral morphine equivalents, cumulative

次要结局

  • Pain at Rest(Postoperative Day 1,2,3,7,90)
  • Opioid Side Effects(Postoperative Day 1,2)
  • Neuropathic Pain Assessed With S-LANSS(Postoperative Day 7, Postoperative Day 90)
  • Patient Satisfaction(Postoperative Day 1,2,3,7)
  • Post-operative Pain(Postoperative Day 1)
  • Pain With Activity(Postoperative Day 1,2,3,7,90)
  • Readiness for Discharge Time(From end of surgery until the date/time of first documented clearance for discharge, assessed up to 1 week.)
  • Blinding Assessment(Assessed on day of discharge and on seventh post operative day)
  • Opioid Consumption During the First 3 Days Post-op(Postoperative day 0,1,2,3)
  • Quality of Recovery(Postoperative Day 1,2,3)
  • No Opioids Consumed(0 to 24 hours post-operatively)

研究者

发起方
Hospital for Special Surgery, New York
申办方类型
Other
责任方
Sponsor

研究点 (1)

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