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Effect of ultrasound-guided transversus abdominis plane block under oblique costal margin on postoperative sleep quality in patients undergoing laparoscopic upper abdominal surgery

Effect of ultrasound-guided transversus abdominis plane block under oblique costal margin on postoperative sleep quality in patients undergoing laparoscopic upper abdominal surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091604
Enrollment
Unknown
Registered
2024-10-31
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

Postoperative sleep disorders, upper abdominal surgery, nerve block, postoperative analgesia

Interventions

Oblique costal inferior transversus abdominis plane block ( ropivacaine ) group:Ultrasound-guided subcostal transversus abdominis plane block was performed with 0.375 % ropivacaine 20 ml 30 min before
Oblique costal inferior transversus abdominis plane block ( ropivacaine + dexmedetomidine ) group:Ultrasound-guided subcostal transversus abdominis plane block was performed with 0.375 % ropivacaine +
Blank control group:No nerve block was performed before operation, and intravenous inhalation combined anesthesia was routinely maintained. 50 mg flurbiprofen axetil was injected intravenously when th

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ( 1 ) Patients scheduled for elective upper abdominal ( stomach ) surgery ; ( 2 ) Age 18-75 years old.

Exclusion criteria

Exclusion criteria: ( 1 ) suffering from chronic pain syndrome ; ( 2 ) BMI > 35kg / m2 ; ( 3 ) Coagulation dysfunction ; ( 4 ) liver or kidney failure ; ( 5 ) Patients with different types of sleep disorders before surgery ; ( 6 ) local anesthetic allergy ; ( 7 ) The use of chronic opioids ; ( 8 ) Reject the experimenter ; ( 9 ) Pre-existing neurological defects or neuropathy affecting the thoracic and lumbar plexus ; ( 10 ) ASA grade IV or higher patients ; (11) Patients with different types of mental disorders or extremely nervous and difficult to sleep before surgery

Design outcomes

Primary

MeasureTime frame
Sleep quality on the first day after operation;Postoperative sleep quality for 7 consecutive days.;

Secondary

MeasureTime frame
The changes of heart rate at 4 time points during operation.;Sufentanil dosage during operation;Intraoperative dosage of remifentanil;Resting state pain score within 48 hours after operation;Activity pain score within 48 hours after operation;Duration of postoperative analgesia ( the time between the completion of the operation and the first pain at the surgical site );Postoperative nausea and vomiting ( PONV ) at 24 h.;The number of PCA compressions at 48 hours after operation.;Postoperative quality of recovery score ( QoR-15 ) for 7 consecutive days.;The first feeding time after operation;The first postoperative exhaust time;Postoperative first defecation time;Hospitalization time;

Countries

China

Contacts

Public ContactLiu Su

Department of Anesthesiology, Affiliated Hospital of Xuzhou Medical University

150040009@qq.com+86 180 5226 8817

Outcome results

None listed

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