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A clinic application of preoperative ultrasound-guided bilateral continuous transversus abdominis plane block in abdominal surgery

A clinic application of preoperative ultrasound-guided bilateral continuous transversus abdominis plane block in abdominal surgery

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IIR-16009187
Enrollment
Unknown
Registered
2016-09-10
Start date
2016-04-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

gastric cancer and colorectal cancer

Interventions

the laparoscope colon cancer surgery:Combined general anesthesia and Preoperative abdominal transverse plane block
the laparoscope colon cancer surgery:Combined general anesthesia and Preoperative epidural block block
gastric cancer surgery:Combined general anesthesia and preoperative abdominal transverse plane block
gastric cancer operation:Combined general anesthesia and preoperative epidual block
the laparoscope gastric cancer surgery:Combined general anesthesia and preoperative abdominal transverse plane block
the laparoscope gastric cancer surgery:Combined general anesthesia and Preoperative epidural block block

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Elective laparoscope gastric and colon cancer patients and patients with radical gastric cancer surgery, ASA I-II level, aged 18 to 75 years old, body mass index of 18 to 24 kg/m2.

Exclusion criteria

Exclusion criteria: Coagulant function abnormality, alcohol, opioids and other history of analgesic drug dependence, long-term use of history of psychiatric drugs, blood coagulation dysfunction, severe liver and kidney disease, and abnormalities of cardiopulmonary function, peripheral neuropathy and innervation area paresthesia, language communication obstacles, operation time more than 6 hours or more.

Design outcomes

Primary

MeasureTime frame
Intraoperative hemodynamics;VAS scores;The dosage of propofol and remifentanyl;Time of extracted the tube and add analgesic drug;Time before taking liquid meal;Time of pull the urine tube;Length of hospital stay after operation;Time before far;the postoperative hypotension;

Countries

China

Contacts

Public ContactLiu jing-chen

The First Affiliated Hospital of Guangxi Medical University

liujcnn@163.com+86 13978619092

Outcome results

None listed

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