Skip to content

Perioperative Muscle Relaxant and Postoperative Outcomes

Effect of Perioperative Muscle Relaxant Model on Postoperative Outcomes in Chinese Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04371588
Acronym
POMPO
Enrollment
999
Registered
2020-05-01
Start date
2018-03-17
Completion date
2021-08-12
Last updated
2022-09-02

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

Conditions

Postoperative Complications

Keywords

muscle relaxant, general anesthesia, Chinese patient

Brief summary

Muscle relaxant is usually needed for surgery. However, the optimal depth of neuro-muscular blockade is still on debate. Deep neuro-muscular blockade may benefit the patients during surgery, but may increase the risk of residual blockade after surgery. Residual blockade has been reported to increase risk of morbidity. In this study, we tend to observe the postoperative outcomes in patients undergoing abdominal surgery under general anesthesia. And to compare the outcomes in patients received different depth of neuro-muscular blockade.

Interventions

OTHERNo Response to Train of Four Stimulation

No response is observed during Train of Four stimulation monitoring during surgery

OTHER1-2 Response to Train of Four Stimulation

1 to 2 response is observed during Train of Four stimulation monitoring during surgery

Sponsors

Air Force Military Medical University, China
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Age ≥18 years old * Body mass \<18 kg/m2 * American Society of Anesthesiologists status I-II * Patients scheduled for elective laparoscopic colorectal or urological surgery * Patients received general anesthesia and muscle relaxant * Patients with written informed consent.

Exclusion criteria

* Second surgery during the same admission. * Outpatient surgery * Retroperitoneal laparoscopic surgery * Patients scheduled for mechanical ventilation after surgery * Patients scheduled for muscle relaxant other than rocuronium * Patients with pregnancy or planned for breeding * Patients who are involved in other studies

Design outcomes

Primary

MeasureTime frameDescription
Visual Analogue Scale of pain at rest at 24 hours after surgeryfrom end of surgery to 24 hours after surgeryThe intensity of pain is reported by the patient by provide a number between 0 and 10. 0 means no pain, and 10 means unbearable pain. Higher score means stronger pain.
Visual Analogue Scale of pain at cough at 24 hours after surgeryfrom end of surgery to 24 hours after surgeryThe intensity of pain is reported by the patient by provide a number between 0 and 10. 0 means no pain, and 10 means unbearable pain. Higher score means stronger pain.

Secondary

MeasureTime frameDescription
Time to extubation of the endotracheal tubefrom end of surgery to removal of the endotracheal tube, on an average of 15 minutes
Incidence of patients suffering pain at 24 hours after surgeryfrom end of surgery to 24 hours after surgery
Satisfaction score of the Surgeon to the condition during surgeryfrom start of surgery to end of surgery, on an average of 2.5 hoursThe satisfaction of the Surgeon is measured by a scale from 0-10. 0 is for extremely unsatisfied, 10 is for totally satisfied. Higher score means higher satisfaction. The surgeon is asked to give a number between 0 and 10 to describe his satisfaction.
Incidence of major postoperative complicationsfrom end of surgery to discharge from the hospital, on an average of 5 daysIncidence of major postoperative complications (including myocardial ischemia, pulmonary infection, respiratory failure, brain ischemia)
Time to flatusfrom end of surgery to flatus, on an average of 3 days

Countries

China

Outcome results

None listed

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