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Comparison of Dexmedetomidine and Meperidine for the Prevention of Shivering Following Coronary Artery Bypass Graft

Comparison of Dexmedetomidine and Meperidine for the Prevention of Shivering Following Coronary Artery Bypass Graft: Study Protocol of a Randomized Controlled Trial

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04735965
Enrollment
180
Registered
2021-02-03
Start date
2021-07-15
Completion date
2022-08-31
Last updated
2022-01-10

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

Conditions

Coronary Artery Disease, Postoperative Shivering

Keywords

Shivering

Brief summary

This study aims to compare the effects of dexmedetomidine and meperidine on the incidence of shivering in patients undergoing CABG.

Detailed description

Shivering is a common complication in the postoperative period. The incidence of shivering has been reported to range from 5% to 65% under general anesthesia and as 33% during epidural anesthesia. Shivering can increase perioperative risk in patients. Both dexmedetomidine and meperidine are effective agents for the prevention of postanesthetic shivering. However, few studies have compared the anti-shivering effects of different agents following coronary artery bypass graft (CABG). This study aims to compare the effects of dexmedetomidine and meperidine on the incidence of shivering in patients undergoing CABG.

Interventions

DRUGDexmedetomidine

Dexmedetomidine would be intravenously infused at a dose of 1μg/kg over 15 minutes 30 min before the end of surgery

DRUGMeperidine

Meperidine would be intravenously injected at a dose of 0.5mg/kg 30 min before the end of surgery

DRUGPlaceb

Equal volume of normal saline to dexmedetomidine and meperidine group.

Sponsors

Qianfoshan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

(1) aged between 18 and 75 years, (2) undergoing elective CABG, (3) ASA grade of II-IV, and (4) in accordance with ethical guidelines, patients must voluntarily participate in the trial and sign the informed consent for the clinical study.

Exclusion criteria

(1) patients with neurological or psychiatric disorders, (2) hepatic and renal dysfunction, (3) severe hyperthyroidism or hypothyroidism, (4) a body temperature greater than 38 °C or less than 36 °C, (5) postoperative hemodynamic instability, (6) preoperative use of a left ventricular assistance device, (7) pa severe diabetic complications (diabetic ketoacidosis, hyperosmolar coma, various infections, diabetic nephropathy), (8) participation in other clinical studies within the past 3 months, (9) acute or chronic pain, (10) addiction to opioids, (11) drug abuse, (12) pain management, and (13) neuromuscular disease, (14) on-pump CABG.

Design outcomes

Primary

MeasureTime frameDescription
The incidence of postoperative shiveringWithin postoperative 24 hoursThe incidence and severity of postoperative shivering and the rescue treatment

Secondary

MeasureTime frameDescription
The incidence of postoperative hypotension and bradycardiaFrom the administration of experimental drugs to postoperative 24 hours
Ramsay sedation scoreWithin postoperative 3 daysThe minimum and maximum score are 1 and 6, respectively. Score 1 represents that patients is anxious and agitated or restless , or both. And score 6 represents that patients exhibits no response.
Postoperative extubation timeThe time of extubation
Length of stay in the ICUThe length of stay in ICU within postoperative 30 days
Times of postoperative rescue drugs usedWithin postoperative 24 hours
The incidence of postoperative arrhythmiasWithin postoperative 24 hours
The incidence and severity of postoperative PONVWithin postoperative 3 days
Length of stayThe first day after surgery to discharge
The rate of all-cause death of participantsWithin postoperative 30 days
The incidence of postoperative deliriumWithin postoperative 7 days

Countries

China

Contacts

Primary ContactCuicui Cao
cccbzyxy@163.com+8615863187590

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026