Skip to main content
Clinical Trials/NCT05715684
NCT05715684
Recruiting
Not Applicable

Patient-Centered Surgical Prehabilitation

Dana-Farber Cancer Institute2 sites in 1 country25 target enrollmentMarch 1, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bladder Cancer
Sponsor
Dana-Farber Cancer Institute
Enrollment
25
Locations
2
Primary Endpoint
Length of stay
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

The purpose of this research is to validate the prehabilitation program which is defined as a set of interventions meant to prepare the body physically and nutritionally for the cystectomy procedure.

Detailed Description

This research study is testing the efficacy of the prehabilitation study which is a set of investigational interventions and also tries to define the most appropriate and effective set type of interventions to use for further studies. "Investigational" means that the intervention is being studied. In this research study, the investigators hope to learn whether or not this combination of prehabilitation interventions has an impact on the recoverability of participants who will undergo cystectomy or bladder removal surgery. The 5 interventions that make up the prehabilitation study are: * Participant Interview (If one of the first ten participants) * Exercise Testing * Exercise Training * Nutritional Support * Clinical Assessment of Nutritional Status

Registry
clinicaltrials.gov
Start Date
March 1, 2023
End Date
December 25, 2027
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Matthew Mossanen, MD

Urologic Surgeon

Dana-Farber Cancer Institute

Eligibility Criteria

Inclusion Criteria

  • Patents must be candidates for all types of cystectomy surgery including urinary diversion via open or robotic approach.
  • Patients between the ages 18 and 85 years
  • American Society of Anesthesiologists (ASA) Physical Status Score of class 1-4
  • Ileal conduit or ileal neobladder urinary diversion
  • Able to understand the study procedures, agreed to participate in the study program, and voluntarily provided informed consent

Exclusion Criteria

  • Scheduled for a partial cystectomy
  • Previous total colectomy, gastrectomy, or gastric bypass, or functional colostomy or ileostomy
  • More than three doses of opioids (oral or parenteral) within 7 days before the day of surgery
  • The presence of metastatic cancer
  • Be undergoing treatment for another type of cancer concurrently
  • Chemotherapy for bladder cancer within 1 month of scheduled surgery; prior neoadjuvant chemotherapy allowed.
  • Pregnant (identified by a positive serum pregnancy test administered after the initial screening process and before the commencement of study activities) or lactating, or not postmenopausal (no menses for at least 1 year) and of childbearing potential and not using an accepted method of birth control (i.e, surgical sterilization; intrauterine contraceptive device; oral contraceptive, diaphragm, or condom in combination with contraceptive cream, jelly, or foam; or abstinence) (Participants will be asked to use birth control for the entire study and for at least 2 weeks after the last dose of study drug.)
  • Participated in another investigational drug or medical device study within 30 days of surgery or planning to be enrolled in another investigational drug or medical device study or any study in which active patient participation was required outside normal hospital data collection during the course of this study
  • Clinically significant laboratory abnormalities at screening that would have resulted in the cancellation of surgery
  • Using illicit drugs or abusing alcohol

Outcomes

Primary Outcomes

Length of stay

Time Frame: 60 months

This is the total length of stay in days after bladder removal surgery

Number and type of minor and major complications

Time Frame: 60 months

This is the number and types of major and minor complications which occur post bladder removal surgery

Total days hospitalized within 30-days of surgery

Time Frame: 60 months

This is the total number of days within 30 days after bladder removal surgery, that a patient is hospitalized.

Discharge disposition

Time Frame: 60 months

This is the disposition of the patient at discharge or when the patient is released from the hospital.

Readmissions

Time Frame: 60 months

This is the number of times a patient that was discharged come back to the hospital for any issue related to their bladder removal surgery.

Study Sites (2)

Loading locations...

Similar Trials