RECRUITING

Growth Hormone for the Treatment of Gastroparesis

Conditions

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 study is to determine whether treatment with Growth Hormone results in symptomatic improvement in patients with gastroparesis.

Official Title

Low-dose Growth Hormone for the Treatment of Gastroparesis

Quick Facts

Study Start:2024-10-22
Study Completion:2027-10
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06803589

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. * Symptoms \> 6 months that have not responded satisfactorily to standard treatment.
  2. * For gastroparesis: Gastroparesis Cardinal Symptom Index (GCSI) score of \>21
  1. * Known history of GH deficiency, hypothalamic or pituitary disease
  2. * Diabetes
  3. * Prior use of GH therapy
  4. * Age-adjusted low serum IGF1
  5. * Women on oral estrogen therapy6
  6. * Pregnancy or nursing
  7. * History of malignant solid tumors
  8. * Obesity (BMI \> 30)History of coronary and thromboembolic diseases.
  9. * History of sarcoidosis
  10. * History of pituitary surgery
  11. * History of thyroid nodules.
  12. * Any other condition, which in the opinion of the investigator would impede compliance or hinder completion of the study.
  13. * Failure to give informed consent.

Contacts and Locations

Study Contact

Guillermo GI Program Coordinator, Research
CONTACT
480-301-4679
barahona.guillermo@mayo.edu
Tisha Lunsford, MD
CONTACT
lunsford.tisha@mayo.edu

Principal Investigator

Tisha Lunsford
PRINCIPAL_INVESTIGATOR
Mayo Clinic

Study Locations (Sites)

Mayo Clinic
Phoenix, Arizona, 85054
United States
Mayo Clinic in Arizona
Scottsdale, Arizona, 85259
United States

Collaborators and Investigators

Sponsor: Mayo Clinic

  • Tisha Lunsford, PRINCIPAL_INVESTIGATOR, Mayo Clinic

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 Date2024-10-22
Study Completion Date2027-10

Study Record Updates

Study Start Date2024-10-22
Study Completion Date2027-10

Terms related to this study

Additional Relevant MeSH Terms

  • Gastroparesis