Guangzhou General Hospital of Guangzhou Military Command
Guangzhou, Guangdong, 510010, China
NCT Number: NCT03221491
In this study, the investigators investigated the efficacy, usefulness and analgesic consumption of three different patient-controlled analgesia(PCA) programmes:bolus dose alone without background infusion, bolus dose with low background infusion and bolus dose with high background infusion to evaluate postoperative analgesia for patients after laparoscopic colorectal surgery.
Looking for future studies?
Notify Me18 year–65 year
All sexes
Interventional
Not applicable
Guangzhou, Guangdong, 510010, China
There have been many studies using patient-controlled analgesia (PCA) and opioids for postoperative analgesia.Patient-controlled analgesia with opioids is now widely used after surgery for the treatment of acute postoperative pain. This technique provides effective pain treatment, adjusts the dose according to personal need and keeps plasma analgesic levels at a constant level,but the incidence of opioid-induced side-effects still be reported frequently.A proper PCA programme may increase efficiency of analgesic and decrease incidence of analgesic-induced side-effects.
In this study, 90 patients who is undergoing elective laparoscopic colorectal surgery will be randomly allocated into three groups (no background infusion group(Group B0),low background infusion group(Group B1) and high background infusion group(Group B2)). Patients in all groups will be given a patient-controlled analgesia (PCA) pump in post anesthetic recovery unit (PACU) after surgery.The PCA programme of Group B0 is dezocine 0.6mg/kg, flubiprofen 3mg/kg, diluted into 120ml and administer at a background infusion of 0ml/h, and a bolus of 4ml, with a lock-out of 15min. The PCA protocol of Group B1 is dezocine 0.6mg/kg,flubiprofen 3mg/k diluted into 120ml and administer at a background infusion of 1ml/h, and a bolus of 2ml, with a lock-out of 15min.The PCA protocol of Group B2 is dezocine 0.6mg/kg,flubiprofen 3mg/k diluted into 120ml and administer at a background infusion of 2ml/h, and a bolus of 2ml, with a lock-out of 15min.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients receive analgesic regimens using Patient-Controlled Analgesia(PCA) with different background infusion.
Time frame: At 24 hours after surgery
The total consumption of dezocine during 24 hours after surgery are recorded.
Time frame: At 24 hours and 48 hours after surgery
Measure whether nausea and vomiting exist and the level of severity.
Time frame: At 0, 2, 4, 8, 24, 48 and 72 hours after surgery
Measure sedation level by using ramsay sedation score.
Time frame: At 0, 2, 4, 8, 24, 48 and 72 hours after surgery
Pain scores at rest and movement are evaluated with a numeric rating scale (NRS)
Weifeng Tu
Other
Comparison of Intravenous Patient-Controlled Analgesia With Different Background Infusion After Colorectal Surgery
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07361822
Agnosia, Nervous System Diseases
Beijing, China
View Trial DetailsNCT06000137
Patient-Controlled Analgesia
Shanghai, Shanghai Municipality, China
View Trial DetailsNCT04082039
Patient-Controlled Analgesia, Total Laparoscopic Hysterectomy
Seoul, South Korea
View Trial DetailsNCT00564603
Abdominal Surgeries, Neurologic Manifestations
Nanjing, Jiangsu, China
View Trial Details