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Liposomal bupivacaine used for quadratus lumborum block to promote postoperative gastrointestinal functional recovery in patients undergoing colorectal surgery: a prospective, randomized controlled clinical study

Liposomal bupivacaine used for quadratus lumborum block to promote postoperative gastrointestinal functional recovery in patients undergoing colorectal surgery: a prospective, randomized controlled clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080543
Enrollment
Unknown
Registered
2024-01-31
Start date
2024-02-01
Completion date
Unknown
Last updated
2024-02-05

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

Conditions

Colorectal disease

Interventions

liposomal bupivacaine group (LB group):0.65% liposomal bupivacaine 20ml will be used for quadratus lumborum block.
Ropivacaine group (R group):0.2% ropivacaine 20ml will be used for quadratus lumborum block.

Sponsors

Peking University Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Age 18-90 years old; Both men and women; ASA GradeI-III; BMI<40kg/m²; Patients who are undergoing colorectal surgery under general anesthesia and have signed informed consent.

Exclusion criteria

Exclusion criteria: Coagulation abnormalities, infection/inflammation at the puncture site, allergy to liposomal bupivacaine or ropivacaine, a clear or known history of spinal deformation or spinal surgery, and a history of chronic pain, patients with intestinal obstruction, refused to sign the informed consent.

Design outcomes

Primary

MeasureTime frame
First postoperative exhaust time;

Secondary

MeasureTime frame
Intake, feeling nauseated, emesis, exam, and duration of symptoms scoring system (I-FEED) score;Incidence of postoperative gastrointestinal dysfunction (POGD);visual analogue scale (VAS) score of pain at rest/activity;Additional doses of opioids;Occurrence and severity of postoperative nausea and vomiting (PONV);Type and dosage of additional antiemetic drugs;Time to get out of bed for the first time;Duration of postanesthesia care unit (PACU);Duration of postoperative length of stay (LOS); QOR-15 score during hospitalization;

Countries

China

Contacts

Public ContactXinhai Wu

Peking University Shenzhen Hospital

45130096@qq.com+86 136 8880 2432

Outcome results

None listed

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