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Application and mechanism study of buccal needle therapy combined with transversus abdominis plane block in postoperative analgesia for patients undergoing laparoscopic sleeve gastrectomy

Application and mechanism study of buccal needle therapy combined with transversus abdominis plane block in postoperative analgesia for patients undergoing laparoscopic sleeve gastrectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126728
Enrollment
Unknown
Registered
2026-06-15
Start date
2026-06-20
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Metabolic syndrome

Interventions

Control:Simulated acupuncture combined with transversus abdominis plane block
Buccal needle combined group:Buccal acupuncture combined with transversus abdominis plane block

Sponsors

Huai'an First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18y-60y, ASA?-?, volunteer to participate in this study and sign the informed consent; 2. All met the diagnosis of metabolic syndrome and underwent surgery.

Exclusion criteria

Exclusion criteria: 1. There are serious cardiovascular system diseases and insufficiency of liver and kidney functions. 2. Patients with mental disorders or those who have difficulty communicating and cooperating. 3. Patients with cheek defects, trauma, or those who refuse acupuncture.

Design outcomes

Primary

MeasureTime frame
The dosage of sufentanil during the operation;The recovery quality of the patients at 24 hours and 48 hours after the operation;The level of plasma TNF-a in patients;The level of plasma ß -endorphin in patients;The level of plasma IL-6 in patients;The level of plasma CRP in patients;Visual Analogue Scale;

Secondary

MeasureTime frame
Intraoperative blood loss volume;Analgesia-related adverse reactions-vomiting;The dosage of propofol during the operation;;The length of hospital stay of patients;needle-related adverse reactions-bleeding;Analgesia-related adverse reactions-nausea;Intraoperative intravenous infusion volume;needle-related adverse reactions-fainting during acupuncture;Insomnia Severity Index;Intraoperative urine volume;Analgesia-related adverse reactions-pruritus;The time when the patient first passes gas after the surgery;The dosage of remifentanil during the operation;The number of manual compressions of the postoperative analgesic pump;Analgesia-related adverse reactions-respiratory depression;The patient satisfaction;Extubation time;The time when the patient first gets out of bed and moves around after surgery;The number of remedial analgesics;Needle-related adverse reactions-infection;The names and dosages of the drugs for remedial analgesia;Anesthesia time;

Countries

China

Contacts

Public ContactGao Pengfei

Huai'an First People's Hospital

hayygpf@njmu.edu.cn+86 517 80872261

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 29, 2026