Combined Intravenous Dexamethasone and Dexmedetomidine as Adjuncts to Popliteal and Saphenous Nerve Blocks in Patients Undergoing Orthopaedic Surgery of the Foot and Ankle. A Randomised, Blinded, Placebo-controlled, Parallel Clinical Trial
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 120
- 试验地点
- 2
- 主要终点
- Time to first pain (measured in minutes)
研究概览
简要总结
The investigators will investigate the beneficial and harmful effects of combining dexamethasone (12 mg) and dexmedetomidine (1mcg/kg) as adjuncts to popliteal and saphenous nerve blocks in patients undergoing surgery of their foot or ankle.
详细描述
This is a randomised, blinded, placebo-controlled, multicentre, parallel, 3-arm clinical trial assessing the effects of adjunct intravenous dexamethasone + dexmedetomidine 1mcg/kg versus intravenous dexamethasone 12mg versus intravenous placebo on time to first pain (i.e. block duration) in patients undergoing surgery of the foot or ankle. All participants will receive a sciatic and saphenous nerve block and general anesthesia.
The investigators will randomise participants to either intervention arm. Participants will be allocated according to a computer-generated random allocation sequence with random permuted blocks and stratification by site. The allocation will be concealed in sequentially numbered opaque envelopes that will not be opened before the participant has been allocated to that specific allocation number/envelope. Trained trial personnel not otherwise involved in the trial will prepare the trial medication according to the allocation.
All others involved will be blinded for the entire duration of the trial (participant, carers, investigators, people delivering the intervention, observers/outcome assessors, statisticians). Blinding will not be broken until agreement has been reached within the steering committee regarding the statistical analysis. The trial medication is prepared in identical syringes with 20ml of identically appearing trial medication. The syringes are subsequently marked with 'syringe 1' and 'syringe 2' and delivered to the investigators. Syringe 1 either contains 12mg dexamethasone or saline and will be administered prior to block performance using an infusion pump set to deliver the volume over 12 minutes. Syringe 2 either contains 1 mcg/kg dexmedetomidine or saline and will be administered after block performance and general anesthesia over 30 minutes using an infusion pump, thereby masking the sedative effect of the dexmedetomidine. The investigators will not be present in the operation room during surgery.
The investigators expect little to no attrition bias since the intervention is simple with a short follow-up. The investigators expect some missing data for duration of the motor block, as most participants will have the affected limb immobilized post-surgery, thereby making assessment of return of motor function difficult.
The statistical analysis plan was pre-defined prior to unblinded data becoming available and can be found on: https://doi.org/10.6084/m9.figshare.22491214.
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
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
盲法说明
Trial medication will be prepared by unmasked personnel who are not otherwise involved in the trial. The participant, personnel, caregivers, investigators, outcome assessors, and data analysts will be masked to treatment allocation.
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Scheduled for unilateral osseous surgery of the ankle or foot
- •General anaesthesia with both a popliteal and a saphenous nerve block for postoperative analgesia
- •Age of 18 or above
- •American Society of Anaesthesiologists Physical Status Score of 1 to 3
- •Body Mass Index of 18 to 40, but a minimum weight of 50 kg.
- •For fertile women, negative urine humane choriongonadotropine test and use of safe anti-conception
- •Ability to understand the trial protocol, risks, benefits, and provide signed informed consent
排除标准
- •Inability to read and understand Danish
- •Uncooperativeness (as judged by investigators)
- •Participation in another trial involving medication
- •Allergy to study medication
- •Daily use of opioids above 30 mg/day morphine (or equivalents)
- •Daily use of corticosteroids of more than 5 mg prednisolone equivalents within the past one month
- •Neurological or musculoskeletal disease making block performance impossible (as judged by investigators)
- •Dysregulated diabetes (as judged by investigators)
- •Dysregulated anticoagulants (as judged by investigators)
- •History of drug or alcohol abuse
- •Contraindications for paracetamol or opioids
- •Contraindications to general anaesthesia
- •Other concomitant conditions needing surgery
- •Other concomitant traumatic injuries
研究组 & 干预措施
Placebo
Participants allocated to this arm will have placebo administered intravenously before block performance and placebo administered intravenously after induction of general anaesthesia.
干预措施: Saline (Drug)
Dexamethasone 12 mg
Participants allocated to this arm will have dexamethasone 12 administered intravenously before block performance and placebo administered intravenously after induction of general anaesthesia.
干预措施: Dexamethasone 12 mg (Drug)
Dexamethasone 12 mg + dexmedetomidine 1 mcg/kg
Participants allocated to this arm will have dexamethasone 12 administered intravenously before block performance and dexmedetomidine 1 mcg/kg administered intravenously after induction of general anaesthesia.
干预措施: Dexamethasone 12 mg + dexmedetomidine 1 mcg/kg (Drug)
结局指标
主要结局
Time to first pain (measured in minutes)
时间窗: 72 hours
Time to first pain will be recorded by the patient and measured in minutes as the time to first perceived pain in the surgical area. The patient will be asked to record the time and date of their first perceived pain in their trial log. This date and time will be compared to the date and time of block performance as recorded in the electronic Case Report Form. In the event of the patient not experiencing any pain, the time to first pain will be set to 72 hours.
次要结局
- Proportion of participants with one or more adverse events not considered to be serious(72 hours)
- Quality of sleep (measured on the Numerical Rating Scale) postoperative night 2(48 hours)
- Duration of the motor block (measured in minutes)(72 hours)
- Quality of sleep (measured on the Numerical Rating Scale) postoperative night 1(24 hours)
- Quality of sleep (measured on the Numerical Rating Scale) postoperative night 3(72 hours)
- Proportion of participants with one or more serious adverse events(30 days)