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Search / Trial NCT06816355

Exogenous Sex Hormones and PONV

Launched by RIVERSIDE UNIVERSITY HEALTH SYSTEM MEDICAL CENTER · Feb 4, 2025

Trial Information

Current as of June 27, 2025

Completed

Keywords

Postoperative Nausea And Vomiting Sex Hormone Estrogen Testosterone Transgender

ClinConnect Summary

A retrospective cohort study will be performed using the TriNetX database. Cohorts were defined using Common Procedural Terminology and International Classification of Diseases-10 codes. Separate analyses will be performed for hysterectomies, orchiectomies, and augmentation mammoplasties. Patients will be excluded if they had a history of postoperative nausea and vomiting or a history of neoplasm for which the respective procedure would be indicated (e.g., uterine, cervical, testicular, or breast cancer). Transgender patients will be excluded if not on exogenous hormone therapy and cisgende...

Gender

ALL

Eligibility criteria

  • Hysterectomy Cohort:
  • Inclusion:
  • - Patients who underwent hysterectomies.
  • Exclusion:
  • - Patients who had malignant neoplasm of the uterus, ovarian, cervical, endometrium, or adnexa.
  • Transgender Male Group
  • Inclusion:
  • administered testosterone within 6 months and 1 day before their hysterectomy
  • have one of the following diagnoses: personal history of sex reassignment, gender identity disorders, or transsexualism.
  • Cisgender Female Group
  • Inclusion:
  • - identified as female.
  • Exclusion:
  • administered testosterone within 6 months and 1 day before their hysterectomy
  • have one of the following diagnoses: personal history of sex reassignment, gender identity disorders, or transsexualism.
  • Orchiectomy Cohort:
  • Inclusion:
  • - patients underwent an orchiectomy.
  • Exclusion:
  • - history of malignant neoplasm of the testis, malignant neoplasm of the prostate, Fournier gangrene, or vascular disorders of male genital organs
  • Transgender Female Group
  • Inclusion:
  • administered estrogen within 6 months and 1 day before their orchiectomy
  • have one of the following diagnoses: personal history of sex reassignment, gender identity disorders, or transsexualism.
  • Cisgender Male Group
  • Inclusion:
  • - identified as male.
  • Exclusion:
  • administered estrogen within 6 months and 1 day before their orchiectomy
  • have one of the following diagnoses: personal history of sex reassignment, gender identity disorders, or transsexualism.
  • Augmentation Mammoplasty:
  • Inclusion:
  • - underwent augmentation mammoplasties.
  • Exclusion:
  • - Have diagnosis of malignant neoplasm of the breast .
  • Transgender Female Group
  • Inclusion:
  • administered estrogen within 6 months and 1 day before their augmentation mammoplasty
  • have one of the following diagnoses: personal history of sex reassignment, gender identity disorder, or transsexualism.
  • Cisgender Female Group
  • Inclusion:
  • - Identified as female
  • Exclusion:
  • administered estrogen within 6 months and 1 day before their hysterectomy
  • have one of the following diagnoses: personal history of sex reassignment, gender identity disorders, or transsexualism.

About Riverside University Health System Medical Center

Riverside University Health System Medical Center (RUHS) is a leading healthcare institution committed to advancing medical research and improving patient outcomes through innovative clinical trials. As a comprehensive medical facility, RUHS integrates cutting-edge technology and a multidisciplinary approach to deliver high-quality care while actively engaging in research initiatives across various therapeutic areas. The center is dedicated to fostering collaborations with academic institutions and industry partners, ensuring that trials are conducted with the highest ethical standards and scientific rigor. Through its robust clinical trial program, RUHS aims to contribute to the development of new therapies and enhance the understanding of complex medical conditions.

Locations

Moreno Valley, California, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported