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Effect of dexmedetomidine on plasma ropivacaine concentration in ultrasound guided QLB using QL3 approach in patient undergoing pancreatic surgery

Effect of dexmedetomidine on plasma ropivacaine concentration in ultrasound guided QLB using QL3 approach in patient undergoing pancreatic surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017087
Enrollment
Unknown
Registered
2018-07-11
Start date
2017-12-25
Completion date
Unknown
Last updated
2018-07-16

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

Conditions

Pancreatic tumor

Interventions

QR Group:Ultrasound-guided QLB using 3mg / kg 0.375% of ropivacaine and intravenous infusion of 0.5 mcg / kg dexmedetomidine
QRM Group:Ultrasound-guided QLB using 3mg / kg 0.375% of ropivacaine+ 0.5 mcg / kg dexmedetomidine and intravenous infusion of 0.5 mcg / kg dexmedetomidine
QNS Group:Ultrasound-guided QLB with 0.8 ml / kg normal saline,and intravenous infusion of 0.5 mcg / kg dexmedetomidine

Sponsors

Department of Anesthesiology, Ruijin Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) aged 18 ~ 65 years old; 2) Patients undergoing upper abdominal surgery scheduled for Chevron incision undergoing general anesthesia with an operative time of 4 to 8 h; 3) ASA classification II ~ III level; 4) BMI = 15.0 to 25.0 kg / m2 [BMI = Body Weight (Kg) / Height (m) 2] (2013 American Guidelines on Management of Overweight and Obese Adults); Ethics, Volunteer Participation, Informed Consent Form.

Exclusion criteria

Exclusion criteria: 1) cognitive dysfunction, communication disorders in patients; 2) patients weighing 10 days or have a history of adrenal cortex suppression or have immune system diseases; 10) hypothyroidism; 11) have a history of asthma; 12) reoperation in 3 months; 13) Contraindications or allergies to test drugs and other narcotic drugs; Patients who participated in other studies within 30 days.

Design outcomes

Primary

MeasureTime frame
Plasma concentration of ropivacaine;VAS and Ramsay Score;

Secondary

MeasureTime frame
patient comfort and satisfaction score;postoperative complication;Time index (call the eyes open time, extubation time, discharge time);score;postoperative agitation;postoperative analgesic pump usage;postoperative complication;

Contacts

Public ContactQingsheng Xue

Department of Anesthesiology, Ruijin Hospital

xueqingshengxueyan@163.com+86 13611909814

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026