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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04332627
Other study ID # B-1910/571-004
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date February 24, 2020
Est. completion date May 21, 2020

Study information

Verified date December 2020
Source Seoul National University Bundang Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The quality of recovery in patients who were reversed neuromuscular blockade by using Sumamadex and Neostigmine in laparoscopic cholecystectomy was compared through the QoR(Quality of Recovery)-15 questionnaire.


Description:

Quality of Recovery questionnaire includes five details (Emotional status, Physical comfort, Physiological support, Physical independece, Pain), and is a proven method of reliability, consistency and validity for evaluating recovery from surgery and anesthesia. After laparoscopic cholecystectomy, patients experience various discomforts such as pain, nausea, vomiting, and placebo due to general anesthesia. Neostigmine has side effects such as crampy abdominal pain, nausea and vomiting. In addition, residual neuromuscular blockade was higher in neostigmine compared with sugammadex. Although sugammadex expected to improve patient's recovery, it is still controversial that sugammadex contributes to clinically meaningfull difference compared with neostigmine. Therefore, the aim of our study is comparison of quality of recovery through QoR-15 questionnaire in patients who were reversed neuromuscular blockade by using sugammadex and neostigmine in laparoscopic cholecystectomy.


Recruitment information / eligibility

Status Completed
Enrollment 77
Est. completion date May 21, 2020
Est. primary completion date May 21, 2020
Accepts healthy volunteers No
Gender All
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria: - patients who underwent laparoscopic cholecystectomy aged 20-70 Exclusion Criteria: - neuromuscular disease - allergy to rocuronium, sugammadex, neostigmine - cognitive impairment ( disable to answer the questionnaire ) - refuse to participate

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Sugammadex
sugammadex 2mg/kg or 4mg/kg according to Train-of-four count (TOF 0 : 4mg/kg, TOF 1-4 : 2mg/kg)
Neostigmine
with glycopyrrolate 0.4mg, neostigmine 0.02mg/kg or 0.04mg/kg or 0.05mg/kg according to Train-of-four count (TOF 0 : wait until TOF 2, TOF2-3: 0.05mg/kg, TOF4: 0.04mg/kg)

Locations

Country Name City State
Korea, Republic of Seoul National University Bundang Hospital Seongnam-si Gyeonggi-do

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Bundang Hospital

Country where clinical trial is conducted

Korea, Republic of, 

References & Publications (2)

Hristovska AM, Duch P, Allingstrup M, Afshari A. Efficacy and safety of sugammadex versus neostigmine in reversing neuromuscular blockade in adults. Cochrane Database Syst Rev. 2017 Aug 14;8:CD012763. doi: 10.1002/14651858.CD012763. Review. — View Citation

Stark PA, Myles PS, Burke JA. Development and psychometric evaluation of a postoperative quality of recovery score: the QoR-15. Anesthesiology. 2013 Jun;118(6):1332-40. doi: 10.1097/ALN.0b013e318289b84b. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of Recovery(QoR)-15 questionnaire score the difference of Quality of Recovery(QoR)-15 score between preoperative and postoperative 1 and 2 days (minimum value : 0, maximum value : 150, the higher the score, the better the result) preoperative 1 days to postoperative 2 days
Secondary recovery time from injection of sugammadex or neostigmien to extubation and confirm of adequate spontaneous breathing perioperative - until 48hours
Secondary PACU(post-anesthesia care unit) stay time from entry of PACU to go general ward perioperative - until 48hours
Secondary postoperative pain score postoperative pain score measured by 11-point NRS(numerical rating scale) score (minimum : 0, maximum : 11, the lower the score, the lesser pain) at postoperative 30minutes, 6hours, 24hours
Secondary the incidence of administration of postoperative rescue drug administration of analgesic drug and anti-emetic drug for postoperative management perioperative - until 72hours
Secondary hospital stay days of hospital stay preoperative - until discharge (usually 48 hours to 72hours)
Secondary urinary retention residual urine > 300ml diagnosed by bladder ultrasonography postoperative - until discharge (usually 48 hours to 72hours)
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