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Development and Validation of a Risk Prediction Model for Postoperative Visceral Pain in Abdominal Surgery Patients

C

Chongqing Medical University

Status

Not yet enrolling

Conditions

Postoperative Visceral Pain

Treatments

Other: Observational assessment of clinical outcomes

Study type

Observational

Funder types

Other

Identifiers

NCT07048782
vpclinicaltrial1

Details and patient eligibility

About

This study aims to investigate the factors influencing the risk of postoperative visceral pain in patients undergoing abdominal surgery. The goal is to develop and validate a predictive model for assessing the risk of postoperative visceral pain, in order to guide individualized preoperative interventions and pain management strategies.

Enrollment

1,135 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing elective abdominal surgery under general anesthesia (including gynecological procedures and general surgery such as gastrointestinal, hepatobiliary, etc.);
  • Aged between 18 and 70 years;
  • Classified as American Society of Anesthesiologists (ASA) physical status II-III;
  • Expected surgery duration ≥ 2 hours.

Exclusion criteria

  • History of previous abdominal surgery;
  • Diagnosed with chronic pain;
  • Long-term use of analgesics or other psychotropic medications;
  • Preoperative emergency condition;
  • Presence of severe comorbidities involving major organ systems;
  • Failure to complete postoperative pain follow-up.

Trial design

1,135 participants in 2 patient groups

Retrospective Cohort
Description:
This cohort includes 1000 patients whose data were collected retrospectively from existing medical records. No additional follow-up is planned.
Treatment:
Other: Observational assessment of clinical outcomes
Prospective Cohort
Description:
This cohort includes 135 patients enrolled prospectively and followed for 2 days to collect outcomes and relevant clinical data.
Treatment:
Other: Observational assessment of clinical outcomes

Trial contacts and locations

1

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Central trial contact

Guangyou Duan, PhD

Data sourced from clinicaltrials.gov

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