RECRUITING

ENDOblock: Bilateral Superficial Cervical Blocks With Local Wound Infiltration in Thyroid Surgery

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This is a single center, prospective, double-blinded randomized controlled trial comparing the efficacy of bilateral superficial cervical plexus blocks (BSCPB) with local wound infiltration vs placebo with local wound infiltration in reducing thyroid surgery postoperative pain. Primary outcomes assessed are post operative pain, quality of life/recovery, post operative nausea/vomiting and opioid use.

Official Title

ENDOblock: Do Bilateral Superficial Cervical Blocks With Local Wound Infiltration Decrease Postoperative Pain After Thyroid Surgery

Quick Facts

Study Start:2023-04-17
Study Completion:2024-11
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05805423

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 99 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * undergoing thyroid surgery, either hemi- or total thyroidectomy
  2. * over 18 years-old and
  3. * able to consent for themselves
  1. * have had previous neck surgery
  2. * have coagulation disorders
  3. * on anticoagulants
  4. * are pregnant
  5. * allergic to bupivacaine
  6. * anyone with chronic pain conditions
  7. * has received steroid injections or used opioids/pain medications in the two weeks leading up to surgery
  8. * have a substernal goiters
  9. * undergoing lateral neck lymph node dissection
  10. * unable to take NSAIDs
  11. * kidney dysfunction (defined as GFR \<60) within 90 days of surgery, prohibiting the use of NSAIDs

Contacts and Locations

Study Contact

Alexis L Woods, MD
CONTACT
2794657077
alwoods@ucdavis.edu
Claire E Graves, MD
CONTACT
9167345907
cegraves@ucdavis.edu

Study Locations (Sites)

UC Davis Medical Center
Sacramento, California, 95817
United States

Collaborators and Investigators

Sponsor: University of California, Davis

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-04-17
Study Completion Date2024-11

Study Record Updates

Study Start Date2023-04-17
Study Completion Date2024-11

Terms related to this study

Keywords Provided by Researchers

  • bilateral superficial cervical plexus block
  • post operative pain after thyroidectomy

Additional Relevant MeSH Terms

  • Post Operative Pain
  • Nausea and Vomiting, Postoperative
  • Opioid Use