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efficacy of laparoscopic transversus abdominis plane (TAP) block for postoperative analgesia in laparoscopic gastric sleeve resection: a single center randomized single blinded case control study

efficacy of laparoscopic transversus abdominis plane (TAP) block for postoperative analgesia in laparoscopic gastric sleeve resection: a single center randomized single blinded case control study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073140
Enrollment
Unknown
Registered
2023-07-03
Start date
2023-07-10
Completion date
Unknown
Last updated
2023-07-10

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

Conditions

obesity

Interventions

laparoscopic assisted transversus abdominis plane block group:laparoscopic assisted transversus abdominis plane block
ultrasound-guided transversus abdominis plane block group:ultrasound-guided transversus abdominis plane block
control group:no

Sponsors

Huadong Hospital affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients fully understand and accept laparoscopic sleeve gastrectomy and postoperative analgesia; (2) 18 years old =65 years old; (3) 27.5=BMI < 32.5; (4) Surgery can be considered after comprehensive evaluation if lifestyle changes and medical treatment are difficult to control, and at least 2 components of metabolic syndrome are met, or there are complications; (5) 32.5=BMI; (6) Patients with T2DM still have certain insulin secretion function; (7) No gastroesophageal reflux disease and hiatal hernia; (8) American Society of Anesthesiologists (ASA) score =3.

Exclusion criteria

Exclusion criteria: (1) The patient does not understand, agree or agree to enter the clinical trial; (2) Age >65 years, age <18 years; (3) Esophageal reflux disease and hiatal hernia; (4) The function of B cells in patients with T2DM was basically lost; (5) BMI < 27.5; (6) Patients with gestational diabetes mellitus and some special types of diabetes mellitus; (7) addicted to drugs or alcohol or suffering from uncontrollable mental illness; (8) Intellectual disability or intellectual immaturity, behavior can not control; (9) the expectation of surgery is not in line with the reality; (10) Unwilling to take the risk of potential surgical complications; (11) unable to cooperate with postoperative changes in diet and living habits, poor compliance; (12) Poor general condition, difficult to tolerate general anesthesia or surgery; (13) Laparoscopic weight-loss modification surgery; (14) Laparoscopic bariatric surgery was converted to open surgery; (15) American Society of Anesthesiologists (ASA) score =4.

Design outcomes

Primary

MeasureTime frame
VAS score 24 hours after surgery;

Secondary

MeasureTime frame
The dose of opioid analgesia used after surgery;the first leaving bed time after surgery;hospital stay after surgery;

Countries

china

Contacts

Public ContactJianjun Yang

Huadong Hospital, Fudan University

ayang1230@126.com+86 21 6248 3180

Outcome results

None listed

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