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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00997633
Other study ID # SPECT IK1991:5
Secondary ID
Status Completed
Phase N/A
First received October 16, 2009
Last updated October 16, 2009
Start date May 1991
Est. completion date August 2004

Study information

Verified date October 2009
Source Uppsala University
Contact n/a
Is FDA regulated No
Health authority Sweden: Isotop CommitteeSweden: Regional Ethical Review Board
Study type Observational

Clinical Trial Summary

SPECT was performed in 51 patients after cytoreductive surgery in combination with intraperitoneal chemotherapy. The detected volume was compared to the number of subsequent sequential postoperative intraperitoneal chemotherapy courses that could be performed without further surgical intervention. SPECT data was found to predict feasibility of sequential postoperative intraperitoneal chemotherapy.


Recruitment information / eligibility

Status Completed
Enrollment 51
Est. completion date August 2004
Est. primary completion date August 2004
Accepts healthy volunteers No
Gender Both
Age group 14 Years to 74 Years
Eligibility Inclusion Criteria:

- Cytoreductive surgery and intraperitoneal chemotherapy

- Single-Photon Emission Computed Tomography (SPECT) before the second course of treatment

Study Design

Observational Model: Case-Only


Related Conditions & MeSH terms


Locations

Country Name City State
Sweden Dept of Surgical Sciences, Section of Surgery S-751 85 Uppsala

Sponsors (1)

Lead Sponsor Collaborator
Uppsala University

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Detected volume measured by SPECT compared to the number of subsequent sequential postoperative intraperitoneal chemotherapy courses No
Secondary The relationship between SPECT, feasibility of SPIC (intraperitoneal chemotherapy), and clinical variables No
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