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

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-70
SponsorThe Second Affiliated Hospital of Chongqing Medical University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

History of previous abdominal surgery;

Diagnosed with chronic pain;

Long-term use of analgesics or other psychotropic medications;

Preoperative emergency condition;

Trial population

Patients aged 18 to 70 years who are scheduled to undergo elective abdominal surgery under general anesthesia (including gynecological and general surgeries such as gastrointestinal and hepatobiliary procedures), with an ASA physical status of II to III, and an expected surgery duration of 2 hours or more.

Trial design

Design model

Cohort

Time perspective

Other

Treatments tested in this trial

  • Observational assessment of clinical outcomes

    Other intervention

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

Treatment groups

1,135 Participants
are divided into 2 treatment groups
Group A: Retrospective Cohort1 intervention
Group B: Prospective Cohort1 intervention

Trial outcomes

Primary outcomes

1

Pain intensity after surgery

Pain 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)

Time frame
From end of surgery to 48 hours postoperatively

Secondary outcomes

1

Postoperative Length of Hospital Stay

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.

Time frame
From end of surgery to hospital discharge (up to 30 days)
2

Postoperative Analgesic Use

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.

Time frame
From end of surgery to hospital discharge (up to 30 days)

Other outcomes

Sponsors and contacts

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