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Risk Factors for Early POCD in the Patients With PSM Undergoing CRS-HIPEC

W

Wuhan University

Status

Completed

Conditions

Postoperative Cognitive Dysfunction

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Objectives to investigate the incidence and associated factors for early postoperative cognitive dysfunction in the patients with peritoneal surface malignancies undergoing cytoreductive surgery and hyperthermic intraperitoneal chemo-therapy(CRS-HIPEC).Methods fifty patients aged 18-65 yr were included in the research and were grouped base on the score of neuropsychological assessments which had done in the ward at 7 day before and after the surgery. The investigators monitored various indicators in the perioperative period, such as age, body weight, sex, education, duration of operation, intraoperative blood loss, cardiovascular events, amount of fluid infused per hour. Meanwhile, the concentration of serum amploid A (SAA),IL-1beta,TNF-alpha,HMGB1,S100b,cortisol and Abeta40 were measured at the various stage of the operation and 24 hours after the operation, and the differences of data between postoperative cognitive dysfunction(POCD) and Non-POCD groups were analyzed.

Enrollment

31 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • age < 65 years or >18 years
  • The patients with peritoneal surface malignancies willing to undergo the cytoreductive surgery with hyperthermic intraperitoneal chemotherapy

Exclusion criteria

  • age < 18 years or >65 years
  • several organ function severely abnormal and can not tolerate the surgery,such as suffering from severely anemia, liver and renal function disfunction, heart and cerebrovascular disease
  • cognitive function was assessed by Mini-Mental State Examination (MMSE) at 1 day before operation and the score<23
  • people with neurological and psychiatric disease, such as anxiety, senile dementia, stroke sequela, cerebral hemorrhage, etc
  • psychiatric drug abusers
  • patients reluctant to go along with the trial

Trial design

31 participants in 2 patient groups

postoperative cognitive dysfunction
Description:
Z score\>1.96
non-postoperative cognitive dysfunction
Description:
Z score\<1.96

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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