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Quality of Life After Cytoreductive Surgery and Intraperitoneal Chemotherapy

Recovery of Quality of Life After Cytoreductive Surgery and Intraperitoneal Chemotherapy for Colorectal Cancer and Pseudomyxoma Peritonei

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03503071
Enrollment
0
Registered
2018-04-19
Start date
2018-10-01
Completion date
2025-12-31
Last updated
2026-08-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer Metastatic

Brief summary

Cytoreductive surgery with intraperitoneal chemotherapy is one of the most important treatments for patients with colorectal cancer and peritoneal metastasis. For the best survival rates, complete removal of all metastatic lesions is the most important part of treatment, and various surgical procedures are required for the complete cytoreduction. Therefore, the postoperative morbidity rates are higher than those of localized colon cancer surgeries and patients can experience a prolonged recovery period and deterioration of physical activities over a long period. The aim of this study is to investigate the change of quality of life after cytoreductive surgery and intraperitoneal chemotherapy for colorectal cancer.

Interventions

Cytoreductive surgery and intraperitoneal chemotherapy for colorectal cancer or pseudomyxoma peritonei. Either early postoperative intraperitoneal chemotherapy (EPIC) or hyperthermic intraperitoneal chemotherapy (HIPEC) is used for intraperitoneal chemotherapy.

Sponsors

Kyungpook National University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Colorectal cancer peritoneal metastasis * Pseudomyxoma peritonei * ECOG (Eastern Cooperative Oncology Group) performance status 0-3 * Normal bone marrow, kidney, and liver function * Patient must sign and date the informed consent

Exclusion criteria

* Palliative surgery * Palliative intraperitoneal chemotherapy * Psychotic disorder * Drug abuser

Design outcomes

Primary

MeasureTime frameDescription
Brief pain inventory (BPI)Changes from baseline pain scores at postoperative 12 monthsPain recovery after cytoreductive surgery and intraperitoneal chemotherapy

Secondary

MeasureTime frameDescription
European Organisation for Research and Treatment of Cancer (EORTC) Quality of life questionnaire (QLQ)-C30preoperative, postoperative 3 months, postoperative 6 months, postoperative 12 months, postoperative 24 monthsQualify of life questionnaire for cancer patients
EORTC QLQ for colorectal cancerpreoperative, postoperative 3 months, postoperative 6 months, postoperative 12 months, postoperative 24 monthsQuality of life questionnaire for patients with colorectal cancer
Short-form(SF)-36preoperative, postoperative 3 months, postoperative 6 months, postoperative 12 months, postoperative 24 monthsGlobal measure of health-related quality of life
Postoperative morbidity90 days after surgeryIncidence and degree of surgical and medical complications after surgery
Postoperative mortality90 days after surgeryIncidence of postoperative mortality
Postoperative recovery150 days after surgeryDuration of hospital stay after surgery
Brief pain inventory (BPI)preoperative, postoperative 3 months, postoperative 6 months, postoperative 24 monthsPain recovery after cytoreductive surgery and intraperitoneal chemotherapy

Countries

South Korea

Contacts

PRINCIPAL_INVESTIGATORSoo Yeun Park, MD

Colorectal Cancer Center, Kyungpook National University Chilgok Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 6, 2026