Actively Recruiting

FEMALE
NCT06458361

Identification of Risk Factors and Construction of Prediction Model for Postoperative Intestinal Anastomotic Leakage in Ovarian Cancer

Led by Zhongda Hospital · Updated on 2024-06-13

300

Participants Needed

1

Research Sites

356 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study was a multicenter, retrospective cohort study. Although advancements in surgical techniques have mitigated the incidence of intestinal anastomotic fistula, complete avoidance remains elusive. Anastomotic leakage (AL) complications directly impinge on postoperative quality of life and pose life-threatening risks if inadequately managed. Given AL's adverse prognostic implications and the financial strain on patients' families, identifying its risk factors aids in perioperative risk assessment, enabling timely clinical decisions on interventions to enhance prognosis and curtail adverse outcomes and economic investments.

CONDITIONS

Official Title

Identification of Risk Factors and Construction of Prediction Model for Postoperative Intestinal Anastomotic Leakage in Ovarian Cancer

Who Can Participate

FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with postoperative pathological diagnosis of primary ovarian, fallopian tube or peritoneal cancer
  • Patients undergoing tumour cytoreductive surgery combined with colorectal resection and stage I intestinal anastomosis
  • No history of other malignant tumours
  • Complete case data
Not Eligible

You will not qualify if you...

  • Previous combination of malignant tumours of other organs
  • Comorbidities with serious diseases related to other organs
  • Patients undergoing secondary tumour cytoreduction

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
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Trial Site Locations

Total: 1 location

1

Zhongda Hospital

Nanjing, Jiangsu, China, 210000

Actively Recruiting

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Research Team

Y

Yang Shen, M.D

CONTACT

Y

Yang Shen

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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