RECRUITING

Decreasing Post-Operative Nausea and Vomiting in the Bariatric Surgical Patient

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

From the research and current studies, post-operative nausea and vomiting is a common complaint after bariatric surgery. Nausea relief inhalers could improve post-operative nausea and vomiting without the need for further medications, subsequently reducing the chance of side effects. This study could help improve patient satisfaction and increase the ability of the patient to ambulate after surgery with the use of a nausea relief inhaler.

Official Title

Decreasing Post-Operative Nausea and Vomiting in the Bariatric Surgical Patient

Quick Facts

Study Start:2020-12-23
Study Completion:2024-11-23
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06110416

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 65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age 18 to 65 years old
  2. * Attend the pre-operative class
  3. * Must be able to read English
  4. * Admitted to B4 surgical acute unit
  5. * Surgery after May 31st, 2020
  1. * BMI greater than 60
  2. * Pre-operatively on nausea medication
  3. * Allergy to spearmint, lemon, ginger, and/or cedarwood
  4. * History of Asthma or chronic obstructive pulmonary disease(COPD)
  5. * Patient intubated or sedated for the 24 hours after surgery

Contacts and Locations

Study Contact

Colette Ngo Ndjom, MS
CONTACT
214-947-1280
ClinicalResearch@mhd.com
Zaid Haddadin, MS
CONTACT
214-947-1280
ClinicalResearch@mhd.com

Principal Investigator

Ashley Attaway, RN
PRINCIPAL_INVESTIGATOR
Methodist Mansfield Medical Center

Study Locations (Sites)

Methodist Mansfield Medical Center
Mansfield, Texas, 76063
United States

Collaborators and Investigators

Sponsor: Methodist Health System

  • Ashley Attaway, RN, PRINCIPAL_INVESTIGATOR, Methodist Mansfield Medical Center

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 Date2020-12-23
Study Completion Date2024-11-23

Study Record Updates

Study Start Date2020-12-23
Study Completion Date2024-11-23

Terms related to this study

Additional Relevant MeSH Terms

  • Nausea, Postoperative
  • Vomiting, Postoperative