RECRUITING

Use of a Subcutaneous Catheter for Controlled Ovarian Stimulation

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

Subcutaneous medications are an integral part of controlled ovarian stimulation protocols for in-vitro fertilization (IVF), but daily or twice daily injections are both physically and emotionally burdensome for patients and their partners. This is a feasibility study to evaluate the use of the Neria Guard™ (Unomedical, Convatec) subcutaneous catheter for ovarian stimulation in IVF.

Official Title

Use of a Subcutaneous Catheter for Controlled Ovarian Stimulation

Quick Facts

Study Start:2023-11-02
Study Completion:2024-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05505474

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 45 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Female between 18 and 45 years of age undergoing controlled ovarian stimulation
  1. * none

Contacts and Locations

Study Contact

Rachel S Mandelbaum, MD
CONTACT
6264409161
rachel.mandelbaum@med.usc.edu
Richard J Paulson, MD
CONTACT
6264409161
rpaulson@med.usc.edu

Principal Investigator

Richard J Paulson, MD
PRINCIPAL_INVESTIGATOR
University of Southern California

Study Locations (Sites)

HRC Fertility
Los Angeles, California, 91101
United States

Collaborators and Investigators

Sponsor: University of Southern California

  • Richard J Paulson, MD, PRINCIPAL_INVESTIGATOR, University of Southern California

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 Date2023-11-02
Study Completion Date2024-12-31

Study Record Updates

Study Start Date2023-11-02
Study Completion Date2024-12-31

Terms related to this study

Additional Relevant MeSH Terms

  • Infertility, Female