Patient Guide: The Impact of a Dexmedetomidine Perfusion on Intraoperative Remifentanil Consumption

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 1 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
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Trial ID: NCTNCT06684197
Status: NOT_YET_RECRUITING
Condition: Dexmedetomidine, Total Intravenous Anesthesia, Remifentanil Consumption, Remifentanil, Laparoscopic Abdominal Surgery
Phase: NA

Where You Can Participate

This study is available at 1 location across the country.

Top locations include:
  • • Montréal, Quebec

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The Impact of a Dexmedetomidine Perfusion on Intraoperative Remifentanil Consumption - Join Clinical Trial NCTNCT06684197

How to Join This Clinical Trial - NCTNCT06684197

Learn how to participate in this NA trial studying an investigational therapy for Dexmedetomidine, Total Intravenous Anesthesia, Remifentanil Consumption, Remifentanil, Laparoscopic Abdominal Surgery. Current status: NOT_YET_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Dexmedetomidine, Total Intravenous Anesthesia, Remifentanil Consumption, Remifentanil, Laparoscopic Abdominal Surgery. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Dexmedetomidine, Total Intravenous Anesthesia, Remifentanil Consumption, Remifentanil, Laparoscopic Abdominal Surgery
Treatment Being Tested
Investigational treatment
Study Phase
NA - Research study
Enrollment Status
NOT_YET_RECRUITING
Study Identifier
NCTNCT06684197 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 1 locations. Find a study site near you:

Clinical Research Site

Montréal, Quebec H1T2M4 - Canada

Status: Contact for availability

How to Enroll in This Study

To learn more about participating in this NA clinical trial for Dexmedetomidine, Total Intravenous Anesthesia, Remifentanil Consumption, Remifentanil, Laparoscopic Abdominal Surgery:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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