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

The Effect of Serum Calcium Levels on Postoperative Pain in Patients Undergoing Abdominal Surgery: A Prospective Observational Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06957158
Enrollment
350
Registered
2025-05-04
Start date
2025-07-31
Completion date
2025-12-31
Last updated
2025-06-27

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

Conditions

Postoperative Pain

Keywords

Serum calcium levels, Postoperative pain, Ionized calcium levels

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.

Interventions

DIAGNOSTIC_TESTPeripheral venous blood

Peripheral venous blood was collected before and after the surgery to measure the total serum calcium levels.

DIAGNOSTIC_TESTArterial blood

Arterial blood was collected before anesthesia induction and after removal of the artificial airway to measure ionized calcium levels.

Sponsors

The Second Affiliated Hospital of Chongqing Medical University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
The incidence of pain NRS score ≥6 within 48 hours after surgeryFrom the end of the surgery to 48 hours after surgeryNRS 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

MeasureTime frameDescription
The maximum incisional pain score at 0-12h postoperativelyFrom the end of the surgery to 12 hours after surgeryNRS 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 surgeryNRS 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 surgeryNRS 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 surgeryNRS 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 surgeryNRS 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 surgeryNRS 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 surgeryThe 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 surgeryPCIA opioid consumption was assessed by checking the PCIA electronic system

Countries

China

Contacts

Primary ContactGuangyou Duan, PhD
duangy@hospital.cqmu.edu.cn+86 183 2337 6014

Outcome results

None listed

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