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OpenTrials
Completed

NCT Number: NCT00910468

Robot-Assisted Laparoscopic Myomectomy Is an Improvement Over Laparotomy in Patients With a Limited Number of Fibroids

This is a retrospective, case-control study of 75 patients having undergone a robotic-assisted laparoscopic myomectomy were compared to patients having undergone myomectomy via laparotomy. Both groups had 3 or fewer fibroids confirmed by pre-operative MRI or on final pathology report. Charts were reviewed for surgical and post-operative variables

Completed

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Key information

Sex eligibility

Female

Study type

Observational

Primary location

Mount SInai School of Medicine

New York, 10029, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • uterus less than or equal to 20 weeks in size by office exam and no greater than three intramural fibroids on pre-operative MRI.

Exclusion criteria

  • significant medical problems limiting their ability to undergo a prolonged laparoscopic procedure and could not have had previous uterine surgery.

Treatment and study plan

Robot-assisted Laparoscopic myomectomy

Procedure

Robot-assisted Laparoscopic myomectomy

Primary outcomes

  1. Post-operative variables, including estimated blood loss, length of stay, days to a regular diet and febrile morbidity

    Time frame: 1 day

Sponsors and collaborators

Lead sponsor

Ascher-Walsh, Charles, M.D.

Indiv

Registry information

Important dates

Study start
2005
Primary completion
2008
Study completion
2008
First posted
May 29, 2009
Registry last updated
May 29, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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