RECRUITING

Outcomes After Weight Loss Surgery in Low-Risk Patients

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

The purpose of this research is to determine patient-reported outcomes after weight loss surgery, including changes in health, mood, quality of life, health satisfaction, and emotional health, in low-risk patients. Weight loss surgery has been well studied for patients with body mass index (BMI) 35 kg/m\^2 or more and those with weight-related medical problems who have a BMI 30 kg/m\^2 or more. However, outcomes after weight loss surgery in patients with BMI under 35 kg/m\^2 and without co-morbidities have not been well studied.

Official Title

Evaluation of Patient Reported Outcomes After Weight Loss Surgery in Low-Risk Patients

Quick Facts

Study Start:2022-03-11
Study Completion:2026-01-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05699083

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:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients with BMI between 30 kg/m2 and 34.5 kg/m2 without co-morbidities who are medically cleared to undergo cosmetic weight loss surgery.
  2. * Written informed consent obtained from the subject or the subject's legal representative and the ability for the subject to comply with the requirements of the study.
  1. * Patients who are pregnant.
  2. * Patients with BMI below 30 kg/m2.
  3. * Patients with BMI above 34.5 kg/m2.
  4. * Patients who have co-morbidities including, but not limited to, diabetes mellitus, hypertension, sleep apnea, and degenerative joint disease.
  5. * Patients who are not medically cleared to undergo weight loss surgery.

Contacts and Locations

Study Contact

Negin Fadaee, BS MPH
CONTACT
818-326-5515
negin@drfeiz.com

Principal Investigator

Michael Feizbakhsh, MD
PRINCIPAL_INVESTIGATOR
Dr. Feiz and Associates

Study Locations (Sites)

Dr. Feiz and Associates
Beverly Hills, California, 90210
United States

Collaborators and Investigators

Sponsor: Dr. Feiz & Associates

  • Michael Feizbakhsh, MD, PRINCIPAL_INVESTIGATOR, Dr. Feiz and Associates

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 Date2022-03-11
Study Completion Date2026-01-12

Study Record Updates

Study Start Date2022-03-11
Study Completion Date2026-01-12

Terms related to this study

Keywords Provided by Researchers

  • Outcomes

Additional Relevant MeSH Terms

  • Weight Loss
  • Bariatric Surgery