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The Effect of Serum Calcium Levels on Postoperative Pain: A Prospective Observational Study

Recruiting
Conditions
Postoperative Pain
Registration Number
NCT06957158
Lead Sponsor
The Second Affiliated Hospital of Chongqing Medical University
Brief Summary

This is a prospective observational study. To investigate the effect of serum calcium levels on postoperative pain in patients undergoing abdominal surgery, and to determine whether changes in serum calcium levels are a risk factor for postoperative pain.

Detailed Description

This study aimed to measure the total serum calcium and ionized calcium levels both before and after surgery. Additionally, NRS scores were recorded at different time points.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
350
Inclusion Criteria
  • Aged 18-70 years old
  • American Society of Anesthesiologists Classification I-III
  • Patients undergoing elective abdominal surgery under general anesthesia
  • Patients participate voluntarily and sign an informed consent form
Exclusion Criteria
  • Patients with a history of severe disease
  • Patients with chronic preoperative pain and/or long-term analgesic use
  • Patients with hearing disorders or verbal communication difficulties
  • Patients with psychiatric disorders or cognitive dysfunction
  • Patients requiring mechanical ventilation or ICU admission after surgery
  • Patients with a history of substance or alcohol abuse Patients who could not cooperate with the study for any reason

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The incidence of pain NRS score ≥6 within 48 hours after surgeryFrom the end of the surgery to 48 hours after surgery

NRS score: pain was assessed using a 10-point NRS (range: 0-10, 0 and 10 indicate no pain and the most extreme pain imaginable, respectively)

Secondary Outcome Measures
NameTimeMethod
The maximum incisional pain score at 0-12h postoperativelyFrom the end of the surgery to 12 hours after surgery

NRS score: pain was assessed using a 10-point NRS (range: 0-10, 0 and 10 indicate no pain and the most extreme pain imaginable, respectively)

The maximum incisional pain score at 12-24h postoperativelyFrom 12hours to 24 hours after surgery

NRS score: pain was assessed using a 10-point NRS (range: 0-10, 0 and 10 indicate no pain and the most extreme pain imaginable, respectively)

The maximum incisional pain score at 24-48h postoperativelyFrom 24 hours to 48 hours after surgery

NRS score: pain was assessed using a 10-point NRS (range: 0-10, 0 and 10 indicate no pain and the most extreme pain imaginable, respectively)

The maximum visceral pain score at 0-12h postoperativelyFrom the end of the surgery to 12 hours after surgery

NRS score: pain was assessed using a 10-point NRS (range: 0-10, 0 and 10 indicate no pain and the most extreme pain imaginable, respectively)

The maximum visceral pain score at 12-24h postoperativelyFrom 12 hours to 24 hours after surgery

NRS score: pain was assessed using a 10-point NRS (range: 0-10, 0 and 10 indicate no pain and the most extreme pain imaginable, respectively)

The maximum visceral pain score at 24-48h postoperativelyFrom 24 hours to 48 hours after surgery

NRS score: pain was assessed using a 10-point NRS (range: 0-10, 0 and 10 indicate no pain and the most extreme pain imaginable, respectively)

Whether additional analgesia was administered within 48 hours after surgeryFrom the end of the surgery to 48 hours after surgery

The proportion of patients who received additional analgesia out of the total patient group

Patient-controlled intravenous analgesia opioid consumptionFrom the end of the surgery to 24 hours and 48 hours after surgery

PCIA opioid consumption was assessed by checking the PCIA electronic system

Trial Locations

Locations (1)

The Second Affiliated Hospital of Chongqing Medical University

🇨🇳

Chongqing, Chongqing, China

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