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Spots Global Cancer Trial Database for Implementation of a Rapid Recovery Program in Gynecologic Oncology Surgery: A Pilot Study

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Implementation of a Rapid Recovery Program in Gynecologic Oncology Surgery: A Pilot Study

Official Title: Implementation of a Rapid Recovery Program in Gynecologic Oncology Surgery: A Pilot Study

Study ID: NCT01705288

Study Description

Brief Summary: Over 600,000 hysterectomies are performed annually in the United States. Despite increasing use of less invasive approaches, the majority of hysterectomies are still performed via traditional laparotomy, which can be associated with generally slower recovery and longer lengths of post-operative hospitalization. Rapid Recovery Protocols (RRP) seek to optimize post-surgical morbidity outcomes by returning a patient to normal physiology as quickly as possible following surgery.

Detailed Description: Subjects will be randomly assigned to one of two groups: Rapid recovery protocol (regional anesthesia, pain control options with emphasis on nonsteroidal anti-inflammatory drugs (NSAIDS) over narcotic pain medications, early ambulation, and early enteral feeding) or standard of care (traditional laparatomy and supportive care).

Eligibility

Minimum Age: 19 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: Yes

Locations

Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota, United States

Contact Details

Name: Peter Argenta, M.D.

Affiliation: Masonic Cancer Center, University of Minnesota

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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