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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Retrospective Cohort | This cohort includes 1000 patients whose data were collected retrospectively from existing medical records. No additional follow-up is planned. |
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| Prospective Cohort | This cohort includes 135 patients enrolled prospectively and followed for 2 days to collect outcomes and relevant clinical data. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Observational assessment of clinical outcomes | Other | This is a non-interventional observational study. No treatment or behavioral intervention is administered. |
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| Measure | Description | Time Frame |
|---|---|---|
| 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) | From end of surgery to 48 hours postoperatively |
| Measure | Description | Time Frame |
|---|---|---|
| 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. | From end of surgery to hospital discharge (up to 30 days) |
| Postoperative Analgesic Use |
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Inclusion Criteria:
Exclusion Criteria:
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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.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Guangyou Duan, PhD | Contact | (+86)18323376014 | duangy@hospital.cqmu.edu.cn |
| Name | Affiliation | Role |
|---|---|---|
| Guangyou Duan, PhD | The Second Affiliated Hospital, Chongqing Medical University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Department of Anesthesiology, The Second Affiliated Hospital, Chongqing Medical University | Chongqing | Chongqing Municipality | 400010 | China |
The individual participant data for this study is available from the sponsor on reasonable request through email.
Five years after the study
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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. |
| From end of surgery to hospital discharge (up to 30 days) |