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Study identifier: NCT07419490 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Utero-ovarian Transposition in Patients With Pelvic Malignancies Undergoing Whole Pelvic Radiotherapy

Condition: Colorectal (Colon or Rectal) Cancer · Pelvic Malignancies · Oncofertility  ·  Sponsor: University of South Florida

PhaseNA
Planned participants26
Who can joinFemale, 18 Months to 40 Months
Healthy volunteersNo

About this study

This study is designed as a Phase I clinical trial enrolling female patients aged 18-40 years who have been diagnosed with pelvic malignancies requiring whole pelvic external radiation therapy (WPXRT) and who express interest in preserving fertility and ovarian function. The trial's primary objective is to assess the feasibility and safety of uterine and ovarian transposition (UOT). Premenopausal women under the age of 40 will undergo UOT using a novel minimally invasive approach. Feasibility and safety will be evaluated through standardized postoperative assessments, including: (A) success in mobilizing and repositioning the uterus, ovaries, and fallopian tubes while maintaining vascular integrity; (B) documentation of surgical complications; (C) monitoring the timeliness and adherence to planned WPXRT. To enhance safety and optimize outcomes, intraoperative imaging with indocyanine green fluorescence and Doppler ultrasonography will be employed. Short-term success will be defined by technical success in repositioning the uterus and ovaries with preserved vascular integrity, absence of major surgical complications, and timely initiation and completion of WPXRT. Long-term success will be evaluated by the preservation of fertility. The study's primary objective is also to evaluate surgical, reproductive, and quality-of-life outcomes following UOT. This objective will determine the procedure's efficacy in preserving ovarian and menstrual function and its potential to sup…

This description comes directly from the study's public registry record.

Talk to the study team

Brittani Powell, MPH, CCRP  ·  (813) 974-5638  ·  RSCH-IRB@usf.edu

Jennifer Childress, RN, CCRP  ·  813-844-1053  ·  jchildress@tgh.org

Always discuss trial participation with your own doctor first.

Locations (1)

Tampa General HospitalTampa, Florida, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07419490