ROCC Trial (Cervical Cancer)

ROCC Trial (Cervical Cancer)

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Purpose of this Study

We are doing this study to compare 2 different procedures for treating cervical cancer and find out which approach has the best outcomes for patients. The two procedures that we will compare are open surgery with a single large incision (laparotomy) and robotic assisted laparoscopy (small incision surgery). We do not know which option is preferable in most cases, and we hope this study can help us find out which procedure is the better choice for patients.

Who Can Participate?

Eligibility

Adults ages 18+ who:
  • Are diagnosed with cervical adenocarcinoma, squamous cell carcinoma, or adenosquamous carcinoma
  • Are candidates for surgical treatment of their cancer
For more information about this study, please contact the study team at sarah.linhart@duke.edu.

Age Range

18-110

Sex/Genders

Female (cisgender)
Looking for Healthy Participants
Yes

What is Involved?

Description

If you choose to join this study, you will get a random assignment (like a coin flip) to either have a laparotomy or a robotic assisted laparoscopy.

Locations

Duke University Hospital
Duke Raleigh Hospital

Visit Timing

Weekdays

Compensation

No

Spanish Materials Available

No

Study Details

Full Title

GOG-3043: A Randomized Controlled Trial of Robotic versus Open Radical Hysterectomy for Cervical Cancer (ROCC trial)

Principal Investigator

Emma
Rossi

Protocol Number

PRO00113573

NCT ID

NCT04831580

Phase

N/A

Enrollment Status

Open to Enrollment