RecruitingN/Aketamine

Dexmedetomidine and Ketamine in VATS Surgery

Sponsored by Ciusss de L'Est de l'Île de Montréal

NCT ID
NCT03596424
Target Enrollment
120 participants
Start Date
2018-02-01
Est. Completion
2026-07-01

About This Study

Postoperative pain after VATS surgery is significant and associated with moderate to high post operative morphine requirements, which can cause opioid related side effects and delay postoperative recovery. To reduce this requirement, multimodal analgesia with non opioid medication such as dexmedetomidine and ketamine can be used. These drugs have demonstrated significant opioid-sparing properties after various types of surgeries. However, very little is known about their ability to do so in VATS surgery. Also, their relative opioid-sparing properties have not been compared, and it is not known whether their combined use can lead to an additional opioid-sparing effect. The primary goal of this study will be to determine the impact of a combined intra operative infusion of ketamine and dexmedetomidine on postoperative morphine requirements in patients undergoing elective VATS, compared to both these drugs infused separately. The hypothesis is that this combined infusion will lead to a 30% further reduction in morphine requirements, 24h after surgery, compared to both these drugs infused separately.

Conditions Studied

Postoperative PainOpioid Use

Interventions

  • Ketamine Hydrochloride
  • Dexmedetomidine Hydrochloride
  • dexmedetomidine Hydrochloride and Ketamine Hydrochloride

Eligibility

Age:18 Years - 80 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* Patients aged 18-80 years old
* American Society of Anesthesiology physical status I-III
* Elective Video-Assisted Thoracic Surgery for pulmonary resection

Exclusion Criteria:

* Patients for which a regional anesthesia technique is planned for postoperative analgesia.
* Patients taking beta-blockers preoperatively.
* Patients with chronic pain taking \>60 mg morphine PO daily (or its equivalent).
* Patients taking pregabalin, gabapentin, amitryptillin, nortryptillin and/or duloxetin.
* Documented allergy to ketamine and/or dexmedetomidine.
* Pregnancy
* Inability to give informed consent
* Linguistic barrier.
* Patient refusal

Study Locations (1)

Ciusss
Montreal, Quebec, Canada

Interested in this trial?

Contact the study team to learn more about eligibility and enrollment.

Veronique Brulotte, MD
CONTACT
5142523400veronique.brulotte@umontreal.ca
Nadia Godin, RN
CONTACT
5142523400
View on ClinicalTrials.gov
Data Source
ClinicalTrials.gov

Last updated from source