The Analgesic Efficacy of Dexmedetomidine as a Local Anesthetic Adjunct in Ankle Blocks for Forefoot Surgery. A Dose Ranging Study.
Trial Snapshot
- Phase
- Not Applicable
- Status
- Terminated
- Enrollment
- 12
- Locations
- 1
- Primary Endpoint
- Duration of Analgesia
Study Overview
Brief Summary
Forefoot surgeries involve a relatively short operation usually completed in 1 - 1½ hours, with patients generally being allowed to go home on the same day. Despite this, post-surgery pain is often severe and a delay in the discharge of patients due to difficulty with pain control after the surgery is common.
Performing nerve blocks in association with sedation is the preferred way to provide pain relief and offers important benefits for foot surgeries. With nerve blocks, the requirement for oral painkillers and their associated side effects is reduced. Increasing the duration of local anesthetic action is helpful as it increases the time of pain relief, allowing for a smoother transition to oral pain medications, earlier discharge, and faster recovery.
Recently, Precedex has been considered for its usefulness in prolonging the pain relief produced by nerve blocks. The identified benefits of this particular use include reducing post-surgical pain medications requirements, reducing the incidence of nausea and vomiting, reducing the incidence of sedation from such medication, and diminishing the incidence of respiratory depression (inadequate breathing). Two small studies have also shown that adding dexmedetomidine to nerve block solution results in prolonging pain relief.
The purpose of the study is to examine several doses of dexmedetomidine combined with local anesthetic drugs and determine the best combination for prolonging pain relief, while minimizing potential side effects.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Triple (Participant, Care Provider, Investigator)
Eligibility Criteria
- Ages
- 18 Years to 65 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •English Speaking
- •American Society of Anesthesiologists (ASA) I-III patients
- •Ages 18-65
- •Body Mass Index (BMI) ≤ 38 kg/m2
Exclusion Criteria
- •Preexisting neurological deficits or peripheral neuropathy in the distribution of the sciatic or femoral nerves
- •Known coronary heart disease, congestive heart failure, cardiomyopathies, or arrhythmias
- •Baseline line heart rate < 60 Beats Per Minute (BPM) or baseline systolic blood pressure < 100 mm Hg
- •Medications that reduce heart rate
- •Known liver or renal dysfunction or existing diseases affecting these organs
- •Local infection
- •Contraindication to regional anesthesia
- •Chronic pain disorders
- •History of use of over 30mg oxycodone or equivalent per day
- •Contraindication to a component of multi-modal analgesia
- •Allergy to local anesthetics or dexmedetomidine
- •History of significant psychiatric conditions that may affect patient assessment
- •Pregnancy
- •Inability to provide informed consent
- •Patient refusal
Arms & Interventions
Dex 0.5
Ropivacaine and Lidocaine plus Dexmedetomidine (0.5mg/kg) plus Normal Saline
Intervention: Dexmedetomidine (Drug)
Dex 1.0
Ropivacaine and Lidocaine plus Dexmedetomidine (1.0mg/kg) plus Normal Saline
Intervention: Dexmedetomidine (Drug)
Outcomes
Primary Outcomes
Duration of Analgesia
Time Frame: patients will be followed for two weeks
Patients will be asked about the duration of their analgesia by asking when they first felt pain at the surgical site. Patients will be asked prior to discharge, and routinely during specified phone calls until analgesia wear off
Secondary Outcomes
- Requirements for pain medications; complications(weekly for up to 2 weeks)