We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Results of CRS and Debulking in PMP Patients

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified August 2011 by Uppsala University.
Recruitment status was:  Active, not recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01427101
First Posted: September 1, 2011
Last Update Posted: September 1, 2011
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Uppsala University
  Purpose
The aim of this study was to compare debulking surgery and cytoreductive surgery in patients with Pseudomyxoma Peritonei with respect to efficacy and safety.

Condition
Pseudomyxoma Peritonei

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Comparison Between Cyotreductive Surgery and Debulking Surgery in Patients With Pseudomyxoma Peritonei

Resource links provided by NLM:


Further study details as provided by Uppsala University:

Primary Outcome Measures:
  • Overall survival
    from treatment and forward


Secondary Outcome Measures:
  • morbidity and mortality [ Time Frame: 90 days ]
    mortality is messured during the first 90 postoperative days and morbidity during hospital stay.


Biospecimen Description:
Patients treated from 1993 are included and during these years treatment strategy has changed. The different strategies are compared but its juts one cohort of patients. No completion date are set due to that reports from other centres show that there are longtime survivers in both treatment groups.

Study Start Date: September 1993
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   20 Years to 80 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patients with Pseudomyxoma Peritonei, sceduled for surgical treatment at Uppsala University Hospital.
Criteria

Inclusion Criteria:

  • Patients with radiology histopathology finding of Pseudomyxoma Peritonei

Exclusion Criteria:

  • Preformance status WHO >2 and histopathology shows other origin then Pseudomyxoma Peritonei
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01427101


Sponsors and Collaborators
Uppsala University
Investigators
Principal Investigator: Haile Mahteme, MD, PhD Uppsala University
  More Information

Responsible Party: Uppsala University
ClinicalTrials.gov Identifier: NCT01427101     History of Changes
Other Study ID Numbers: 2007/073-PMP-Andréasson
First Submitted: August 31, 2011
First Posted: September 1, 2011
Last Update Posted: September 1, 2011
Last Verified: August 2011

Keywords provided by Uppsala University:
Pseudomyxoma Peritonei
Cytoreductive surgery
Debulking surgery
Intraperitoneal chemotherapy

Additional relevant MeSH terms:
Pseudomyxoma Peritonei
Neoplasms, Cystic, Mucinous, and Serous
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Neoplasms