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

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

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07048782
Enrollment
1135
Registered
2025-07-02
Start date
2025-07-01
Completion date
2026-01-30
Last updated
2025-07-02

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

Conditions

Postoperative Visceral Pain

Brief summary

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.

Interventions

OTHERObservational assessment of clinical outcomes

This is a non-interventional observational study. No treatment or behavioral intervention is administered.

Sponsors

The Second Affiliated Hospital of Chongqing Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years

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.

Design outcomes

Primary

MeasureTime frameDescription
Pain intensity after surgeryFrom end of surgery to 48 hours postoperativelyPain intensity will be recorded at 6, 12, 24, and 48 hours after surgery. At each time point, the Numerical Rating Scale (NRS) pain score will be assessed both at rest and during coughing. Pain intensity was assessed using number rating scale (0-10, higher score represents worse pain intensity)

Secondary

MeasureTime frameDescription
Postoperative Length of Hospital StayFrom end of surgery to hospital discharge (up to 30 days)The total time from the end of surgery to hospital discharge will be recorded for each patient. The duration will be measured in days (d) and used to assess postoperative recovery.
Postoperative Analgesic UseFrom end of surgery to hospital discharge (up to 30 days)Detailed records will be kept of the types of analgesics administered postoperatively, the total dosage of each drug, and the frequency of use per day. This measure will help assess pain management and medication requirements after surgery.

Countries

China

Contacts

Primary ContactGuangyou Duan, PhD
duangy@hospital.cqmu.edu.cn(+86)18323376014

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026