Overview

Dexmedetomidine Added to Ropivacaine Single Shot vs Continuous Interscalene Nerve Block

Status:
Recruiting
Trial end date:
2023-11-23
Target enrollment:
0
Participant gender:
All
Summary
Arthroscopic shoulder surgery is increasingly performed in an outpatient setting and post-operative pain management is often a real challenge as those surgeries are well recognized for their high level of pain which often affects physical rehabilitation. The interscalene block is a largely used anesthetic technique to perform these surgeries whilst avoiding general anesthesia (GA) and to provide postoperative analgesia. However, the painful period often exceeds the duration of a single shot block, thus affecting patient recovery. Some specialized centers use a continuous catheter and elastomeric pump in order to prolong the duration of analgesia. However, several logistical, professional and financial constraints limit the use of these catheters and pumps in a great number of outpatient centers. On the other hand, perineural dexmedetomidine is increasingly used as an adjuvant to improve block onset, analgesia duration and patient satisfaction. The use of adjuvants such as perineural dexmedetomidine added to a single shot interscalene block appears to be an interesting option to prolong postoperative analgesia without the limitations imposed by a continuous catheter and elastomeric pumps in arthroscopic shoulder surgeries.
Phase:
N/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Ciusss de L'Est de l'Île de Montréal
Treatments:
Dexmedetomidine
Ropivacaine
Criteria
Inclusion Criteria:

- Patients over 18 years old

- ASA status of I-III

- Patients undergoing elective arthroscopic ambulatory shoulder surgery

- Anticipated return home the same day (less than 12 hours in-hospital) in any operating
theater of the CIUSSS.

Exclusion Criteria:

- less than 18 years old

- Patient refusal

- Pregnancy

- Patients with known allergy to local anesthetics

- Contraindication to interscalene brachial plexus nerve block or superficial cervical
plexus block: coagulopathy, contralateral phrenic nerve dysfunction, infection at the
puncture site, severe chronic obstructive pulmonary disease

- Technical inability to proceed with the interscalene brachial plexus nerve block

- Surgery requiring general anesthesia

- Body weight less than 50 kg

- Patient with no family member or caring adult at home during the first 72h
postoperative (contraindication to elastomeric pump)

- Unable to communicate with the investigators, unable to read the questionnaire, unable
to keep track and notes of the medication taken at home

- Significant psychiatric or cognitive condition interfering with the ability to provide
consent or assessment

- Preexisting neurologic deficits or neuropathy affecting the brachial plexus

- Any contra-indication to same-day surgery identified by the pre-operative clinic such
as, but not limited to, any cognitive disorder, any physical limitation other than the
one leading to surgery that might impair the patient to take care of himself/herself
at home, any severe pulmonary or cardiac disorder, bleeding disorder, etc,

- Any cardiac or pulmonary condition that precludes the risk of bradycardia or
hypotension such as but not limited to symptomatic coronary disease, severe aortic
stenosis, moderate to severe pulmonary hypertension, congestive heart failure, second
or third degree block, pre-existing bradycardia (HR lower than 50), pre-existing
hypotension (SBP lower than 100 mmHg), etc.

- History of chronic pain with daily opioid use during the 3 months before surgery