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Effect of ultrasound-guided rectus abdominis nerve block on the outcome of gynecological single hole laparoscopic surgery

Effect of ultrasound-guided rectus abdominis nerve block on the outcome of gynecological single hole laparoscopic surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056147
Enrollment
Unknown
Registered
2022-02-01
Start date
2022-03-01
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Postoperative of gynecological patients with single hole laparoscopy

Interventions

Group P:100mg ropivacaine injection was diluted to 0.2% concentration with 0.9% normal saline. The posterior sheath nerve block of rectus abdominis was performed under ultrasound guidance, and the ana
Group D:100 mg of ropivacaine was diluted to 0.2% with 0.9% normal saline. Ultrasound guided intramuscular rectus abdominis nerve block analgesia was performed, and the analgesia was observed
control group:The patients in the control group were not blocked by RBS after operation, and the ward doctor gave corresponding remedial treatment according to the situation

Sponsors

Shenzhen Hospital of Guangzhou University of Traditional Chinese Medicine (Futian)
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing gynecological single hole laparoscopic surgery under general anesthesia; 2. Over 18 years and under 65 years; 3. ASA grade I-II; 4. The patient was conscious and understood the investigation content; 5. Those who have signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Long term history of receiving analgesic and sedative drugs and drug abuse; 2. Allergy to local anesthetics or opioids; 3. Psychiatric history or non author; 4. Cardiac insufficiency; bradycardia and heart block; impairment of renal function; patients with active liver disease; 5. Severe visual or hearing impairment; 6. Patients who are illiterate and unable to communicate linguistically with their physician; 7. Regional anesthesia contraindications exist.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale,VAS;Daily sleep disturbance score, DSIS;Ramsay sadation scale;

Secondary

MeasureTime frame
Incidence of vomiting;

Countries

China

Contacts

Public ContactZhu Peng

Shenzhen Hospital of Guangzhou University of Chinese Medicine (Futian)

78336326@qq.com+86 13760427702

Outcome results

None listed

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