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Effect of Noise Blocking During General Anesthesia on Postoperative Pain

Effect of Noise Blocking During General Anesthesia on Postoperative Pain in Patients Undergoing Laparoscopic Abdominal Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05540691
Enrollment
90
Registered
2022-09-15
Start date
2022-10-08
Completion date
2023-02-28
Last updated
2023-03-29

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

Conditions

Postoperative Pain

Keywords

noise blocking, Postoperative Pain

Brief summary

To investigate the effect of noise blocking during general anesthesia on postoperative pain in patients undergoing laparoscopic abdominal surgery. The aim of this study was to determine whether noise blocking can reduce postoperative pain, analgesic use, and its possible effects on intraoperative electrocorticogram.

Interventions

Intervention of wearing noise-canceling earphones after general anesthesia

Sponsors

The Second Affiliated Hospital of Chongqing Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Intervention model description

Patients were randomly divided into intervention group(noise blocking) and control group(No noise blocking)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* ASA Classification ⅰ-ⅲ * Patients undergoing elective laparoscopic abdominal surgery under general anesthesia * Voluntarily accept PCIA and signed informed consent

Exclusion criteria

* Patients with previous severe disease * Patients with hearing abnormalities * Patients requiring mechanical ventilation or undergoing epidural catheters or other types of regional anesthesia after surgery * Patients with chronic preoperative pain and/or long-term analgesic use * Patients who could not cooperate with the study for any reason

Design outcomes

Primary

MeasureTime frameDescription
Maximum pain score (NRS score) at 0-24 hours postoperativelyFrom ending of the surgery to 24 hours postoperativelyNRS score: Pain was assessed on a scale of 0-10, with 0 being no pain and 10 being most painful
Pain score (NRS score) at 0-6 hours postoperativelyFrom ending of the surgery to 6 hours postoperativelyNRS score: Pain was assessed on a scale of 0-10, with 0 being no pain and 10 being most painful
Pain score (NRS score) at 6-12 hours postoperativelyFrom 6 hours postoperatively to 12 hours postoperativelyNRS score: Pain was assessed on a scale of 0-10, with 0 being no pain and 10 being most painful
Pain score (NRS score) at 12-24 hours postoperativelyFrom 12 hours postoperatively to 24 hours postoperativelyNRS score: Pain was assessed on a scale of 0-10, with 0 being no pain and 10 being most painful

Secondary

MeasureTime frameDescription
Patient controlled analgesia pump analgesic consumptionFrom the time when the surgery was completed until to 24 hours after surgeryAnalgesic requirements was assessed by recording the volume of patient controlled analgesia pump
Postoperative hyperalgesia after surgeryfrom the 30 minutes before the surgery until to 30 minutes after surgeryPostoperative hyperalgesia was measured by the ratio of pressure pain threshold at time when discharged from postanesthesia care unit compare to before surgery

Countries

China

Outcome results

None listed

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